Draft Consensus Guideline
Good Manufacturing Practice Guide for
Released for Consultation
At Step 2 of the ICH Process, a consensus draft text or guideline, agreed by the appropriate ICH Expert Working Group, is transmitted by the ICH Steering Committee to the regulatory authorities of the three ICH regions (the European Union, Japan and the USA) for internal and external consultation, according to national or regional procedures.
Table of Contents
This document (Guide) is intended to provide guidance regarding good manufacturing practice (GMP) for the manufacturing of active pharmaceutical ingredients (APIs) under an appropriate system for managing quality. It is also intended to ensure that all APIs meet requirements for quality and purity which they purport or are represented to possess.
In this Guide "manufacturing" is defined to include all operations of receipt of materials, production, packaging, repackaging, labelling, relabelling, quality control, release, storage and distribution of APIs and the related controls. In this Guide the term "should" indicates recommendations that are expected to apply unless shown to be inapplicable or replaced by an alternative demonstrated to provide at least an equivalent level of quality assurance. For the purposes of this Guide, the terms "current good manufacturing practices" and "good manufacturing practices" are equivalent.
The Guide as a whole does not cover safety aspects for the personnel engaged in the manufacture, nor aspects of protection of the environment. These controls are inherent responsibilities of the manufacturer and are governed by national laws.
This Guide is not intended to define registration/filing requirements or modify pharmacopeial requirements. This Guide does not affect the ability of the responsible regulatory agency to establish specific registration/filing requirements regarding APIs within the context of marketing/manufacturing authorizations or drug applications. All commitments in registration/filing documents must be met.
1.2 Regulatory Applicability
Within the world community, materials may vary as to the legal classification as an API. When a material is classified as an API in the region or country in which it is manufactured or used in a drug product, it should be produced according to this Guide.
This Guide applies to the manufacture of APIs for use in human drug (medicinal) products including sterile APIs only up to the point immediately prior to the API being rendered sterile. The sterilization and aseptic processing of sterile APIs are not covered by this guidance, but should be performed in accordance with GMP guidelines for drug (medicinal) products as defined by local authorities.
This Guide covers APIs that are manufactured by chemical synthesis, extraction, cell culture/fermentation, or by recovery from natural sources, or any combination of these processes. Specific guidance for APIs manufactured by cell culture/fermentation is described in Section 18. The intermediates and API's produced by recombinant DNA technology will be included for the purpose of this Guide provided they are proteinacious materials.
This Guide excludes all vaccines, whole cells, whole blood and plasma, and APIs derived from them (plasma fractionation). However, it does include APIs that are produced using blood or plasma as raw materials. Note that cell substrates (mammalian, plant, or microbial cells, tissue or animal sources including transgenic animals) and early process steps may be subject to GMP but are not covered by this Guide. In addition, the Guide does not apply to medical gases, bulk-packaged drug (medicinal) products, and manufacturing/control aspects specific to radiopharmaceuticals.
Section 19 contains guidance that only applies to the manufacture of APIs used in the production of drug (medicinal) products specifically for clinical trials (investigational medicinal products).
An "API Starting Material" is a material used in the production of an API which is incorporated as a significant structural fragment into the structure of the API. An API Starting Material may be an article of commerce, a material purchased from one or more suppliers under contract or commercial agreement, or it may be produced in-house. API Starting Materials normally have defined chemical properties and structure.
The company should designate and document the rationale for the point at which production of the API begins. For synthetic processes this is known as the point at which "API Starting Materials" are entered into the process. For other processes (e.g. fermentation, extraction, purification, etc), this rationale should be established on a case by case basis.
From this point on appropriate GMP as defined in this Guide should be applied to these intermediate and/or API manufacturing steps. This would include the validation of critical process steps determined to impact the quality of the API. However it should be noted that the fact that a company chooses to validate a process step does not necessarily define that step as critical.
The guidance in this document would normally be applied to the steps shown in gray in the table on the next page. The table is an example; it does not imply that all steps shown must be completed. The stringency of GMP in API manufacturing should increase as the process proceeds from early API steps to final steps, purification, and packaging. Physical processing of APIs such as granulation, coating or physical manipulation of particle size (e.g. milling, micronizing) should be conducted at least to the standards of this Guide.
This GMP Guide does not apply to steps prior to the introduction of the defined "API Starting Material".
2 Quality Management
2.10 Quality should be the responsibility of all persons involved in manufacturing.
2.11 Each manufacturer should establish, document, and implement an effective system for managing quality that involves the active participation of management and appropriate manufacturing personnel.
2.12 The system for managing quality should encompass the organisational structure, procedures, processes and resources, as well as activities necessary to ensure confidence that the API will meet its intended specifications for quality and purity. All quality related activities should be defined and documented.
2.13 All quality related activities should be recorded at the time they are performed.
2.14 Any deviation from established procedures should be documented and explained. Critical deviations should be investigated, and the investigation and its conclusions should be documented.
2.15 Procedures should exist for notifying responsible management in a timely manner of regulatory inspections, serious GMP deficiencies, product defects and related actions (e.g. quality related complaints, recalls, regulatory actions, etc.).
2.16 There should be a quality unit(s) which is independent of production, and which fulfills both quality assurance (QA) and quality control (QC) responsibilities. This may be in the form of separate QA and QC units or a single individual (or group), depending upon the size and structure of the organization.
2.17 No materials should be released or used before the satisfactory completion of evaluation by the quality unit(s) unless there are appropriate systems in place to allow for such use (e.g. release under quarantine as described in Section 10.20 or the use of raw materials or intermediates pending completion of evaluation).
2.18 The persons authorised to release intermediates and APIs should be specified.
2.2 Responsibilities of the Quality Unit(s)
2.20 The quality unit(s) should be involved in all quality-related matters.
2.21 The quality unit(s) should review and approve all appropriate quality related documents.
10.50 The main responsibilities of the independent quality unit(s) / should not be delegated. These responsibilities should be described in writing, and should include but not necessarily be limited to:
1. Releasing or rejecting all APIs;
2. Establishing a system to release or reject raw materials, intermediates, packaging and labelling materials;
3. Reviewing completed manufacturing records for critical process steps before release of the API for distribution;
4. Making sure that critical deviations are investigated and resolved;
5. Approving all specifications and master production instructions;
6. Approving all procedures potentially impacting the quality of intermediates or APIs;
7. Making sure that internal audits (self-inspections) are performed;
8. Approving intermediate and API contract manufacturers;
9. Approving changes that potentially impact intermediate or API quality;
10. Reviewing and approving validation protocols and reports;
11. Making sure that quality related complaints are investigated and resolved;
12. Making sure that effective systems are used for maintaining and calibrating critical equipment;
13. Making sure that materials are appropriately tested and the results are reported;
14. Making sure that there is stability data to support retest or expiry dates and storage conditions on intermediates and/or APIs where appropriate; and
15. Performing product quality reviews (as defined in Section 2.5)
2.3 Responsibility for production activities
The responsibility for production activities should be described in writing, and should include but not necessarily be limited to:
1. Preparing, reviewing, approving and distributing the instructions for the production of intermediates or APIs according to written procedures;
2. Producing APIs and, when appropriate, intermediates according to pre-approved instructions;
3. Reviewing all production batch records and ensuring that these are completed and signed;
4. Making sure that all production deviations are reported and evaluated and that critical deviations are investigated and the conclusions are recorded;
5. Making sure that production facilities are clean and when necessary disinfected;
6. Making sure that the necessary calibrations are performed and records kept;
7. Making sure that the premises and equipment are maintained and records kept;
8. Making sure that validation plans, protocols and reports are reviewed and approved;
9. Evaluating proposed changes in product, process or equipment; and
10. Making sure that new and, when appropriate, modified facilities and equipment are qualified.
2.4 Internal Audits (Self Inspection)
2.40 In order to verify compliance with the principles of GMP for APIs, regular internal audits should be performed in accordance with an approved schedule.
2.41 Audit findings and corrective actions should be documented and brought to the attention of responsible management of the firm. Agreed corrective actions should be completed in a timely and effective manner.
2.5 Product Quality Review
2.50 Regular quality reviews of APIs should be conducted with the objective of verifying the consistency of the process. Such reviews should normally be conducted and documented annually and should include at least:
- A review of critical in-process control and critical API test results;
- A review of all batches which failed to meet established specifications;
- A review of all critical deviations or non-conformances and related investigations;
- A review of any changes carried out to the processes or analytical methods;
- A review of results of the stability monitoring program;
- A review of all quality related returns, complaints and recalls; and
- A review of adequacy of corrective actions.
2.51 The results of this review should be evaluated and an assessment made of whether corrective action or any revalidation is necessary. The necessity for such corrective action should be documented. Agreed corrective actions should be completed in a timely and effective manner.
3.1 Personnel Qualifications
3.10 There should be an adequate number of personnel qualified by appropriate education, training and/or experience to perform and supervise the manufacture of intermediates and APIs.
3.11 The responsibilities of all personnel engaged in the manufacture of intermediates and APIs should be specified in writing.
3.12 Training should be regularly conducted by qualified individuals and should cover at a minimum the particular operations that the employee performs and GMP as it relates to the employee's functions. Records of training should be maintained. The practical effectiveness of the training should be periodically assessed.
3.2 Personnel Hygiene
3.20 Personnel should practice good sanitation and health habits.
3.21 Personnel should wear clean clothing suitable for the manufacturing activity with which they are involved and this clothing should be changed when necessary. Additional protective apparel, such as head, face, hand, and arm coverings, should be worn when necessary, to protect intermediates and APIs from contamination.
3.22 Personnel should avoid direct contact with intermediates or APIs.
3.23 Smoking, eating, drinking, chewing and the storage of food should be restricted to certain designated areas separate from the manufacturing areas.
3.24 Personnel suffering from an infectious disease or having open lesions on the exposed surface of the body should not engage in activities, that could result in compromising the quality of APIs. Any person shown at any time (either by medical examination or supervisory observation) to have an apparent illness or open lesions that may adversely affect the safety or quality of APIs should be excluded from direct contact with APIs until the condition is corrected or qualified medical personnel determine that the person's inclusion would not jeopardize the safety or quality of the APIs.
3.30 Consultants advising on the manufacture and control of intermediates or APIs should have sufficient education, training, and experience, or any combination thereof, to advise on the subject for which they are retained.
3.31 Records should be maintained stating the name, address, qualifications, and type of service provided by these consultants.
4 Buildings and Facilities
4.1 Design and Construction
4.10 Buildings and facilities used in the manufacture of intermediates and APIs should be located, designed, and constructed to facilitate cleaning, maintenance, and operations as appropriate to the type and stage of manufacture. Facilities should also be designed to minimize potential contamination. Where microbiological specifications have been established for the intermediate or API, facilities should also be designed to limit exposure to objectionable microbiological contaminants as appropriate.
4.11 Buildings and facilities should have adequate space for the orderly placement of equipment and materials to prevent mix-ups and contamination.
4.12 Where the equipment itself (e.g., closed or contained systems) provides adequate protection of the material, such equipment may be located outdoors.
4.13 The flow of materials and personnel through the building or facilities should be designed to prevent mix-ups or contamination.
4.14 There should be defined areas or other control systems for the following activities:
- Receipt, identification, sampling, and quarantine of incoming materials, pending release or rejection;
- Quarantine before release or rejection of intermediates and APIs;
- Sampling of intermediates and APIs;
- Holding rejected materials before further disposition (e.g., return, reprocessing or destruction);
- Storage of released materials;
- Production operations;
- Packaging and labelling operations; and
- Control and laboratory operations.
4.15 Adequate and clean washing facilities should be provided for personnel. These washing facilities should be equipped with hot and cold water as necessary, soap or detergent, air driers or single service towels. The washing and toilet facilities should be separate from, but easily accessible to, manufacturing areas. Adequate facilities for showering and/or changing clothes should be provided when appropriate.
4.16 Laboratory areas/operations should normally be separated from production areas. Some laboratory areas, in particular those used for in-process controls, may be located in production areas, provided the operations of the production process do not adversely affect the accuracy of the laboratory measurements, and the laboratory and its operations do not adversely affect the production process or intermediate or API.
4.20 All utilities that could impact on product quality (e.g. steam, gases, and compressed air) should be qualified and appropriately monitored to ensure that specifications are met and action is taken when limits are exceeded.
4.21 Adequate ventilation and exhaust systems should be provided, where necessary. These systems should be designed and constructed to minimise risks of contamination and cross-contamination and should include equipment for control of air pressure, microorganisms (if appropriate), dust, humidity, and temperature, as appropriate to the stage of manufacture. Particular attention should be given to areas where APIs are exposed to the environment.
4.22 If air is recirculated to production areas, appropriate measures should be taken to control risks of contamination and cross-contamination.
4.23 Permanently installed pipework should be appropriately identified. This can be accomplished by identifying individual lines, documentation, computer control systems, or alternative means. Pipework should be located to avoid risks of contamination of the intermediate or API.
4.24 Drains should be of adequate size and should be provided with an air break or a suitable device to prevent back-siphonage, when appropriate.
4.30 Water used in the manufacture of APIs should be demonstrated to be suitable for its intended use.
4.31 Unless otherwise justified, process water should, at a minimum, meet national standards for potable water that have been documented as at least equivalent to World Health Organization (WHO) guidelines. In the absence of national standards, WHO guidelines should be used.
4.32 If potable water standards are insufficient to assure API quality and tighter chemical and microbiological water quality specifications are necessary, appropriate specifications for physical/chemical attributes, total microbial counts, objectionable organisms and/or endotoxins should be established.
4.33 Where water used in the process is treated by the manufacturer to achieve defined quality, the treatment process should be validated and monitored with appropriate action limits.
4.34 Where the manufacturer of a non-sterile API either intends or claims that it is suitable to be used in further processing to produce a sterile drug (medicinal) product, then water used in the final isolation and purification steps should be monitored and controlled for total microbial counts, objectionable organisms, and endotoxins.
4.40 Dedicated production areas, which may include such facilities as air handling equipment and/or process equipment, should be employed in the production of each type of highly sensitizing material (e.g., penicillins or cephalosporins).
4.41 Dedicated production areas should also be considered when material of an infectious nature or high pharmacological activity or toxicity is involved (e.g., certain steroids or cytotoxic anti-cancer agents) unless validated inactivation and/or cleaning procedures are established and maintained.
4.42 Appropriate measures should be established and implemented to prevent cross-contamination from personnel, materials, etc. moving from one dedicated area to another.
4.43 Any production activities (including weighing, milling, or packaging) of highly toxic non-pharmaceutical materials such as herbicides and pesticides should not be conducted using the buildings and/or equipment being used for the production of APIs. Handling and storage of these highly toxic non-pharmaceutical materials should be separate from APIs.
4.50 Adequate lighting should be provided in all areas to facilitate cleaning, maintenance, and proper operations.
4.6 Sewage and Refuse
4.60 Sewage, refuse, and other waste (e.g., solids, liquids, or gaseous by-products from manufacturing) in and from buildings and the immediate surrounding area should be disposed of in a safe, timely, and sanitary manner. Containers and/or pipes for waste material should be clearly identified.
4.7 Sanitation and Maintenance
4.70 Buildings used in the manufacture of intermediates and APIs should be properly maintained and repaired and kept in a clean condition.
4.71 Written procedures should be established assigning responsibility for sanitation and describing the cleaning schedules, methods, equipment, and materials to be used in cleaning buildings and facilities.
4.72 When necessary, written procedures should also be established for the use of suitable rodenticides, insecticides, fungicides, fumigating agents, and cleaning and sanitizing agents to prevent the contamination of equipment, raw materials, packaging/labelling materials, intermediates, and APIs.
5 Process Equipment
5.1 Design and Construction
5.10 Equipment used in the manufacture of intermediates and APIs should be of appropriate design and adequate size, and suitably located for its intended use, cleaning, sanitization (where appropriate), and maintenance.
5.11 Equipment should be constructed so that surfaces that contact raw materials, intermediates, or APIs do not alter the quality of the intermediates and APIs beyond the official or other established specifications.
5.12 Production equipment should only be used within its qualified operating range.
5.13 Major equipment (e.g., reactors, storage containers) and permanently installed processing lines used during the production of an intermediate or API should be appropriately identified.
5.14 Any substances necessary for the operation of equipment, such as lubricants, heating fluids or coolants, should not contact intermediates or APIs so as to alter their quality beyond the official or other established specifications. Any deviations from this should be evaluated to ensure that there are no detrimental effects upon the fitness for purpose of the material. Wherever possible food grade lubricants and oils should be used.
5.15 Closed or contained equipment should be used whenever appropriate. Where open equipment is used, or equipment is opened, appropriate precautions should be taken to minimize contamination.
5.16 A set of current drawings should be maintained for equipment and critical installations (e.g., instrumentation and utility systems).
5.2 Equipment Maintenance and Cleaning
5.20 Schedules and procedures (including assignment of responsibility) should be established for the preventative maintenance of equipment.
5.21 Written procedures should be established for cleaning of equipment and its subsequent release for use in the manufacture of intermediates and APIs. Cleaning procedures should contain sufficient details to enable operators to clean each type of equipment in a reproducible and effective manner. These procedures should include, but should not be limited to:
- Assignment of responsibility for cleaning of equipment;
- Cleaning schedules, including, where appropriate, sanitizing schedules;
- A complete description of the methods and materials, including dilution of cleaning agents used to clean equipment;
- When appropriate, instructions for disassembling and reassembling each article of equipment to ensure proper cleaning;
- Instructions for the removal or obliteration of previous batch identification;
- Instructions for the protection of clean equipment from contamination prior to use;
- Inspection of equipment for cleanliness immediately before use, if practical; and
- Establishing the maximum time that may elapse between the completion of processing and equipment cleaning, when appropriate.
5.22 Equipment and utensils should be cleaned, stored, and, where necessary, sanitized or sterilized to prevent contamination or carry-over of a material that would alter the quality of the intermediate or API beyond the official or other established specifications.
5.23 Where equipment is assigned to continuous production or campaign production of successive batches of the same intermediate or API, equipment should be cleaned at appropriate intervals to prevent build-up and carry-over of contaminants (e.g. degradants) or objectionable levels of micro-organisms.
5.24 Non-dedicated equipment should be cleaned between production of different materials to prevent cross-contamination.
5.25 Acceptance criteria for residues and the choice of cleaning procedures and cleaning agents should be defined and justified.
5.26 Equipment should be identified as to its contents and its cleanliness status by appropriate means.
5.30 Control, weighing, measuring, monitoring and test equipment that is critical for assuring the quality of intermediates or APIs should be calibrated according to written procedures and an established schedule.
5.31 Equipment calibrations should be performed using standards traceable to certified standards, if existing.
5.32 Records of these calibrations should be maintained.
5.33 The current calibration status of critical equipment should be known and verifiable.
5.34 Instruments that do not meet calibration criteria should not be used.
5.35 Deviations from approved standards of calibration on critical instruments should be investigated to determine if these could have had an impact on the quality of the intermediate(s) or API(s) manufactured using this equipment since the last successful calibration.
5.4 Computerized Systems
5.40 GMP related computerized systems should be validated. The depth and scope of validation depends on the diversity, complexity and criticality of the computerized application.
5.41 Appropriate installation qualification and operational qualification should demonstrate the suitability of computer hardware and software to perform assigned tasks.
5.42 Commercially available software that has been qualified does not require the same level of testing. If an existing system was not validated at time of installation, a retrospective validation may be conducted if appropriate documentation is available.
5.43 Computerized systems should have sufficient controls to prevent unauthorized access or changes to data. There should be controls to prevent omissions in data (e.g. system turned off and data not captured). There should be a record of any data change made, the previous entry, who made the change, and when the change was made.
5.44 Written procedures should be available for the operation and maintenance of computerized systems.
5.45 Where critical data are being entered manually, there should be an additional check on the accuracy of the entry. This may be done by a second operator or by the system itself.
5.46 Incidents related to computerized systems that could affect the quality of intermediates or APIs or the reliability of records or test results should be recorded and investigated.
5.47 All changes to the computerized system should be made according to a change procedure and should be formally authorized, documented and tested. Records should be kept of all changes including modifications and enhancements made to the hardware, software and any other critical component of the system to demonstrate that the final system is maintained in a validated state.
5.48 If system breakdowns or failures would result in the permanent loss of records then a back-up system should be provided. A means of ensuring data protection should be established for all computerized systems.
5.49 Recording data by a second means in addition to the computer system is acceptable to provide a backup data source.
6 Documentation and Records
6.1 Documentation System and Specifications
6.10 All documents related to the manufacture of intermediates or APIs should be prepared, reviewed, approved and distributed according to written procedures. Such documents may be in paper or electronic form.
6.11 The issuance, revision, superseding and withdrawal of all documents should be controlled with maintenance of revision histories.
6.12 A procedure should be established for retaining all appropriate documents (e.g., development history reports, scale-up reports, technical transfer reports, process validation reports, training records, production records, control records, and distribution records). The retention periods for these documents should be specified.
6.13 All production, control, and distribution records should be retained for at least one year after the expiry date of the batch. For APIs with retest dates, records should be retained for at least three years after the batch is completely distributed.
6.14 When entries need to be made in records, these should be made indelibly in spaces provided for such entries, directly after performing the activities (in the order performed), and should identify the person making the entry. Corrections to entries should be dated and signed and leave the original entry still readable.
6.15 All records or copies of such records, should be readily available during the retention period at the establishment where the activities described in such records occurred. Records that can be promptly retrieved from another location by electronic or other means are acceptable.
6.16 Specifications, instructions, procedures, and records may be retained either as originals or as true copies such as photocopies, microfilm, microfiche, or other accurate reproductions of the original records. Where reduction techniques such as microfilming or electronic records are used, suitable retrieval equipment and a means to produce a hard copy should be readily available.
6.17 Specifications should be established and documented for raw materials, intermediates where necessary, APIs and labelling and packaging materials. In addition, specifications may be necessary for certain other materials, such as process aids, gaskets, or other materials used during the production of intermediates or APIs that would critically impact on quality. Acceptance criteria should be established and documented for in-process controls.
6.18 Electronic signatures on documents are acceptable, provided they are authenticated and secure.
6.2 Equipment Cleaning and Use Record
6.20 Records of major equipment use, cleaning, sanitization and/or sterilization and maintenance should show the date, time (if appropriate), product, and batch number of each batch processed in the equipment, and the person who performed the cleaning and maintenance.
6.21 If equipment is dedicated to manufacturing one intermediate or API, then individual equipment records are not necessary if batches of the intermediate or API follow in traceable sequence. In cases where dedicated equipment is employed, the records of cleaning, maintenance, and use may be part of the batch record or may be maintained separately.
6.3 Records of Raw Materials, Intermediates, API Labelling and Packaging Materials
6.30 Records should be maintained including:
- The name of the manufacturer, identity and quantity of each shipment of each batch of raw materials, intermediates or labelling and packaging materials for API's; the name of the supplier; the supplier's control number(s), if known, or other identification numbe; the number allocated on receipt; and the date of receipt; -
- The results of any test or examination performed and the conclusions derived from this;
- Records tracing the use of materials;
- Documentation of the examination and review of API labelling and packaging materials for conformity with established specifications; and
- The final decision regarding rejected raw materials, intermediates or API labelling and packaging materials.
6.31 Master (approved) labels should be maintained for comparison to issued labels.
6.4 Master Production Instructions (Master Production and Control Records)
6.40 To ensure uniformity from batch to batch, master production instructions for each intermediate and API should be prepared, dated, and signed by one person and independently checked, dated, and signed by a person in the quality unit(s).
6.41 Master production instructions should include:
- The name of the intermediate or API being manufactured and an identifying document reference code, if applicable;
- A complete list of raw materials and intermediates designated by names or codes sufficiently specific to identify any special quality characteristics;
- An accurate statement of the quantity or ratio of each raw material or intermediate to be used, including the unit of measure. Where the quantity is not fixed, the calculation for each batch size or rate of production should be included. Reasonable variations are permitted provided they are justified;
- The production location and major production equipment to be used;
- Detailed production instructions, including the:
- sequences to be followed,
- ranges of process parameters to be used,
- sampling instructions and in-process controls with their acceptance criteria, where appropriate,
- time limits for completion of individual processing steps and/or the total process, where appropiate; and
- expected yield ranges at appropriate phases of processing or time;
- Where appropriate, special notations and precautions to be followed, or cross-references to these; and
- The instructions for storage of the intermediate or API to assure its suitability for use, including the labelling and packaging materials and special storage conditions with time limits where appropriate.
6.5 Batch Production Records (Batch Production and Control Records)
6.50 Batch production records should be prepared for each intermediate and API and should include complete information relating to the production and control of each batch. The batch production record should be checked before issuance to assure that it is the correct version and a legible accurate reproduction of the appropriate master production instruction. If the batch production record is produced from a separate master document, that document must include a reference to the current master production instruction being used.
6.51 These records should be numbered with a unique batch or identification number, dated and signed when issued. In continuous production the product code together with the date and time may serve as the unique identifier until the final number is allocated.
6.52 Written procedures should be established and followed for investigating critical deviations or the failure of a batch of intermediate or API to meet specifications. The investigation should extend to other batches that may have been associated with the specific failure or deviation.
6.53 Intermediates and APIs failing to meet established specifications should be identified as such and quarantined. Written procedures should be followed if these materials are reprocessed or reworked. The final disposition of rejected materials should be recorded.
6.54 Documentation of completion of each significant step in the batch production records (batch production and control records) should include:
- Dates and, when appropriate, times;
- Identity of major equipment (e.g., reactors, driers, mills, etc.) used;
- Specific identification of each batch, including weights, measures, and batch numbers of raw materials, intermediates, or any reprocessed materials used during manufacturing;
- Actual results recorded for critical process parameters;
- Any sampling performed;
- Signatures of the persons performing and directly supervising or checking each critical step in the operation;
- In-process and laboratory test results;
- Actual yield at appropriate phases or times;
- Description of packaging and label for intermediate or API;
- Representative label of API or intermediate if made commercially available;
- Any deviation noted, its evaluation, investigation conducted (if appropriate) or reference to that investigation if stored separately; and
- Results of release testing.
6.6 Laboratory Control Records
6.60 Laboratory control records should include complete data derived from all tests necessary to ensure compliance with established specifications and standards, including examinations and assays, as follows:
- A description of samples received for testing, including the material name or source, batch number or other distinctive code, date sample was taken, and, where appropriate, the quantity and date the sample was received for testing;
- A statement of or reference to each test method used;
- A statement of the weight or measure of sample used for each test as described by the method; data on or cross-reference to the preparation and testing of laboratory reference standards, reagents and standard solutions,
- A complete record of all raw data secured during each test, in addition to graphs, charts, and spectra from laboratory instrumentation, properly identified to show the specific material and batch tested;
- A record of all calculations performed in connection with the test, including, for example, units of measure, conversion factors, and equivalency factors;
- A statement of the test results and how they compare with established specifications;
- The signature of the person who performed each test and the date(s) the tests were performed; and
- The date and signature of a second person showing that the original records have been reviewed for accuracy, completeness, and compliance with established standards.
6.61 Complete records should also be maintained for:
- Any modifications to an established analytical method,
- Periodic calibration of laboratory instruments, apparatus, gauges, and recording devices;
- All stability testing performed on APIs; and
- Out-of-specification (OOS) investigations.
6.7 Batch Production Record Review
6.70 Written procedures should be established and followed for the review and approval of batch production and laboratory control records, including packaging and labelling, to determine compliance of the intermediate or API with established specifications before a batch is released or distributed.
6.71 Batch production and laboratory control records for critical process steps should be reviewed and approved by the quality unit(s) before an API batch is released or distributed. Production and laboratory control records for earlier, non-critical process steps may be reviewed by qualified production personnel or other units following procedures approved by the quality unit(s).
6.72 All deviation, investigation, and OOS reports should be reviewed as part of the batch record review before the batch is released.
6.73 The quality unit(s) may delegate to the production unit the responsibility and authority for release of intermediates.
7 Materials Management
7.1 General Controls
7.10 There should be written procedures describing the receipt, identification, quarantine, storage, handling, sampling, testing, and approval or rejection of materials.
7.11 Manufacturers of intermediates and/or APIs should have a system for evaluating the suppliers of critical materials.
7.12 Materials should be purchased against an agreed specification, from a supplier or suppliers approved by the quality unit(s).
7.13 If the supplier of a critical material is not the manufacturer of that material, the name and address of that manufacturer should be known by the intermediate and/or API manufacturer.
7.14 Changing the source of supply of critical raw materials should be treated according to Section 13, Change Control.
7.2 Receipt and Quarantine
7.20 Upon receipt and before acceptance, each container or grouping of containers of materials should be examined visually for correct labelling, container damage, broken seals and evidence of tampering or contamination. Materials should be held under quarantine until they have been sampled, examined or tested as appropriate, and released for use.
7.21 Before incoming materials are mixed with existing stocks (e.g., solvents or stocks in silos) they should be identified as correct and released. Procedures should be available to prevent discharging into the wrong stock.
7.22 If bulk deliveries are made in non-dedicated tankers, there should be assurance of no cross-contamination from the tanker. Means of providing this assurance could include one or more of the following:
- certificate of cleaning
- testing for trace impurities
- audit of the supplier.
7.23 Large storage containers, and their attendant manifolds, filling and discharge lines should be appropriately identified.
7.24 Each container or grouping of containers (batches) of materials should be assigned and identified with a distinctive code, batch, or receipt number. This number should be used in recording the disposition of each batch. A system should be in place to identify the status of each batch.
7.3 Sampling and Testing of Materials
7.30 At least one test to verify the identity of each batch of material should be conducted, with the exception of the materials described below in 7.32. A supplier's Certificate of Analysis may be used in place of performing other tests provided that the manufacturer has a system in place to evaluate suppliers.
7.31 Supplier approval should require an evaluation including adequate evidence (e.g., past quality history) that the supplier can consistently provide material meeting specifications. Full analyses should be conducted on at least three batches before reducing in-house testing. However, as a minimum, a full analysis should be performed at appropriate intervals and compared with the Certificates of Analysis. Reliability of Certificates of Analysis should be checked at regular intervals.
7.32 Processing aids, hazardous or highly toxic raw materials, and other special materials do not need to be tested, provided the manufacturer's Certificate of Analysis is obtained showing that these raw materials conform to established specifications. Visual examination of containers, labels, and recording of batch numbers should help in establishing the identity of these materials. The lack of on-site testing for these materials should be justified and documented.
7.33 Samples should be representative of the batch of material from which they are taken. Sampling methods should specify the number of containers to be sampled, which part of the container to sample, and the amount of material to be taken from each container. The number of containers to sample and the sample size should be based upon a sampling plan which takes into consideration criticality of the material, material variability, past quality history of the supplier, and the quantity needed for analysis.
7.34 Sampling should be conducted at defined locations and by procedures designed to prevent contamination of the material sampled and contamination of other materials.
7.35 Containers from which samples are withdrawn should be opened carefully and subsequently reclosed. They should be marked to indicate that a sample has been taken.
7.40 Materials should be handled and stored in a manner to prevent degradation, contamination, and cross-contamination.
7.41 Materials stored in fiber drums, bags, or boxes should be stored off the floor and when necessary, suitably spaced to permit cleaning and inspection.
7.42 Materials should be stored under conditions and for a period that have no adverse affect on their quality, and should normally be rotated so that the oldest stock is used first.
7.43 Certain materials in suitable containers may be stored outdoors, provided identifying labels remain legible and containers are appropriately cleaned before opening and use.
7.44 Rejected materials should be identified and controlled under a quarantine system designed to prevent their unauthorised use in manufacturing.
7.50 Materials should be re-evaluated as appropriate to determine their suitability for use (e.g., after prolonged storage or exposure to heat or humidity).
8 Production and In-Process Controls
8.1 Production Operations
8.10 Raw materials for intermediate and API manufacturing should be weighed or measured under appropriate conditions that do not affect their suitability for use. Weighing and measuring devices should be of suitable accuracy for the intended use.
8.11 If a material is subdivided for later use in production operations, the container receiving the material should be suitable and should be so identified that the following information is available:
- Material name and item code;
- Receiving or control number;
- Weight or measure of material in the new container; and
- Re-evaluation or retest date if appropriate.
8.12 Critical weighing, measuring, or subdividing operations should be supervised or subjected to an equivalent control. Prior to use, production personnel should verify that the materials are those specified in the batch record for the intended intermediate or API.
8.13 Other critical activities should be supervised or subjected to an equivalent control.
8.14 Actual yields should be compared with expected yields at designated steps in the production process. Expected yields with appropriate ranges should be established based on previous laboratory, pilot scale, or manufacturing data. Deviations in yield associated with critical process steps should be investigated to determine their impact or potential impact on the resulting quality of affected batches.
8.15 Any deviation should be documented and explained. Any critical deviation should be investigated.
8.16 The processing status of major units of equipment should be indicated either on the individual units of equipment or by appropriate documentation, computer control systems, or alternative means.
8.17 Materials to be reprocessed or reworked should be appropriately controlled to prevent unauthorized use.
8.2 Time Limits
8.20 If time limits are specified in the master production instruction (see 6.41), these time limits should be met to ensure the quality of intermediates and APIs. Deviations should be documented and evaluated. Time limits may be inappropriate when processing to a specification (e.g., pH adjustment, hydrogenation, drying to predetermined specification) because completion of reactions or processing steps are determined by in-process sampling and testing.
8.21 Intermediates held for further processing should be stored under appropriate conditions to assure their suitability for use.
8.3 In-process Sampling and Controls
8.30 Written procedures should be established to monitor the progress and control the performance of processing steps that cause variability in the quality characteristics of intermediates and APIs. In-process controls and their acceptance criteria should be defined based on the information gained during the development stage or historical data.
8.31 The acceptance criteria and type and extent of testing may depend on the nature of the intermediate or API being manufactured, the reaction or process step being conducted, and the degree to which the process introduces variability in the product's quality. Less stringent in-process controls may be appropriate in early processing steps, whereas tighter controls may be appropriate for later processing steps (e.g., isolation and purification steps).
8.32 Critical in-process controls (and process monitoring), including the control points and methods, should be stated in writing and approved by the quality unit(s).
8.33 In-process controls may be performed by production department personnel and the process adjusted without prior quality unit(s) approval, provided adjustments are made within pre-established limits approved by the quality unit(s). All tests and results should be fully documented as part of the batch record.
8.34 Written procedures should describe the sampling methods for in-process materials, intermediates, and APIs. Sampling plans and procedures should be based on scientifically sound sampling practices.
8.35 In-process sampling should be conducted using procedures designed to prevent contamination of the sampled material and other intermediates or APIs. Procedures should be established to ensure the integrity of samples after collection.
8.4 Blending Batches of Intermediates or APIs
10.51 For the purpose of this document, blending is defined as the process of combining materials within the same specification to produce a homogeneous intermediate or API. In-process mixing of fractions from single batches (e.g., collecting multiple fermentation batches in a single holding tank or collecting several centrifuge loads from a single crystallization batch) is considered to be part of the production process and is not considered to be blending.
8.41 Out-Of-Specification batches should not be blended with other batches for the purpose of meeting specifications. Each batch incorporated into the blend should have been manufactured using an established process and should have been individually tested and found to meet appropriate specifications prior to blending.
8.42 Acceptable blending operations include but are not limited to:
- Blending of small batches to increase batch size
- Blending of tailings (i.e., relatively small quantities of isolated material) from batches of the same intermediate or API to form a single batch.
8.43 Blending processes should be adequately controlled and documented and the blended batch should be tested for conformance to established specifications.
8.44 The batch record of the blending process should allow traceability back to the individual batches that make up the blend.
8.45 Where physical attributes of the API are critical (e.g., APIs intended for use in solid oral dosage forms or suspensions) blending operations should be validated to show homogeneity of the combined batch. Validation should include testing of critical attributes (e.g., particle size distribution, bulk density, and tap density) that may be affected by the blending process.
8.46 Stability testing of the final blended batches is necessary if the blending could cause a change in the already established stability data.
8.47 The expiry or retest date of the blended batch should be based on the manufacturing date of the oldest tailings or batch in the blend.
8.5 Contamination Control
8.50 Carryover of leftover materials from successive batches of the same intermediate or API (e.g., residue adhering to the wall of a micronizer, residual layer of damp crystals remaining in a centrifuge bowl after discharge, and incomplete discharge of fluids or crystals from a processing vessel upon transfer of the material to the next step in the process) is acceptable provided it is adequately controlled. Such carryover should not result in the carryover of degradants or microbial contamination that may adversely alter the established API impurity profile.
8.51 Production operations should be conducted in a manner that will prevent contamination of intermediates or APIs by other materials.
8.52 Special attention should be taken when APIs are handled after purification to avoid contamination.
9 Packaging and Labelling of APIs and Intermediates for Transport
9.10 There should be written procedures describing the receipt, identification, quarantine, sampling, examination and/or testing and release, and handling of packaging and labelling materials.
9.11 Packaging and labelling materials should conform to established specifications. Those that do not comply with such specifications should be rejected to prevent their use in operations for which they are unsuitable.
9.12 Records should be maintained for each shipment of labels and packaging materials showing receipt, examination, or testing, and whether accepted or rejected.
9.2 Packaging Materials
9.20 Containers should provide adequate protection against deterioration or contamination of the intermediate or API that may occur during transportation and recommended storage.
9.21 Containers should be clean, and where indicated by the nature of the intermediate or API, sanitized to ensure that they are suitable for their intended use. These containers should not be reactive, additive, or absorptive so as to alter the quality of the intermediate or API beyond the specified limits.
9.22 If containers are re-used, they should be cleaned in accordance with documented procedures and all previous labels should be removed or defaced.
9.3 Label Issuance and Control
9.30 Access to the label storage areas should be limited to authorised personnel.
9.31 Procedures should be used to reconcile the quantities of labels issued, used, and returned and to evaluate discrepancies found between the number of containers labelled and the number of labels issued. Such discrepancies should be investigated, and the investigation should be approved by the quality unit(s).
9.32 All excess labels bearing batch numbers or other batch related printing should be destroyed. Returned labels should be maintained and stored in a manner that prevents mix-ups and provides proper identification.
9.33 Obsolete and out-dated labels should be destroyed.
9.34 Printing devices used to print labels for packaging operations should be controlled to ensure that all imprinting conforms to the print specified in the batch production record.
9.35 Printed labels issued for a batch should be carefully examined for proper identity and conformity to specifications in the master production record. The results of this examination should be documented in the batch production record.
9.36 A printed label representative of those used should be included in the batch production record.
9.4 Packaging and Labelling Operations
9.40 There should be documented procedures designed to ensure that correct packaging materials and labels are used.
9.41 Labelling operations should be designed to prevent mix-ups. There should be physical or spatial separation from operations involving other intermediates or APIs.
9.42 Labels used on containers of intermediates or APIs should indicate the name or identifying code, the batch number of the product and storage conditions when such information is critical to assure the quality of intermediate or API. If the intermediate or API is intended to be transferred outside the control of the manufacturer's material management system, the name and address of the manufacturer, quantity of contents, and special transport conditions and any special legal requirements should also be included on the label. For intermediates or APIs with an expiry date, the expiry date should be indicated on the label and Certificate of Analysis. For intermediates or APIs with a retest date, the retest date should be indicated on the label and/or Certificate of Analysis.
9.43 Packaging and labelling facilities should be inspected immediately before use to ensure that all materials not needed for the next packaging operation have been removed. This examination should be documented in the batch production records, the facility log, or other documentation system.
9.44 Packaged and labelled intermediates or APIs should be examined to ensure that containers and packages in the batch have the correct label. This examination may be part of the packaging operation. Results of these examinations should be recorded in the batch production or control records.
9.45 Intermediate or API containers that are transported outside of the manufacturer's control should be sealed in a manner such that, if the seal is breached or missing, the recipient will be alerted to the possibility that the contents may have been altered.
10 Storage and Distribution
10.1 Warehousing Procedures
10.10 Facilities should be available for the storage of all materials under appropriate conditions (e.g. controlled temperature and humidity when necessary). Records should be maintained of these conditions if they are critical for the maintenance of material characteristics.
10.11 Unless there is an alternative system to prevent the unintentional or unauthorised use of quarantined, rejected, returned, or recalled materials, separate storage areas should be assigned for their temporary storage until the decision as to their future use has been taken.
10.2 Distribution Procedures
10.20 APIs should only be released for distribution to third parties after they have been released by the quality unit(s). API's may be transferred under quarantine to another unit under the company's control when authorized by the quality unit(s) and providing appropriate controls and documentation are in place.
10.21 APIs should be transported in a manner that does not adversely affect their quality.
10.22 Special transport or storage conditions for an API should be stated on the label.
10.23 The API manufacturer should ensure that the contract acceptor (contractor) for transportation of the API knows and follows the appropriate transport and storage conditions.
10.24 A system should be in place by which the distribution of each batch of intermediate and/or API can be readily determined to permit its recall if necessary.
11 Laboratory Controls
11.1 General Controls
11.10 The independent quality unit(s) must have at its disposal adequate laboratory facilities.
11.11 There should be documented procedures describing sampling, testing, approval or rejection of materials, and recording and storage of laboratory data.
11.12 Laboratory records should be maintained in accordance with Section 6.6.
11.13 All specifications, sampling plans, and test procedures should be scientifically sound and appropriate to ensure that raw materials, intermediates, APIs, and labels and packaging materials conform to established standards of quality and/or purity. Specifications and test procedures should be consistent with those included in the registration/filing. There may be specifications in addition to those in the registration/filing. All specifications, sampling plans, and test procedures, including changes to them, should be drafted by the appropriate organizational unit and reviewed and approved by the quality unit(s).
11.14 Appropriate specifications should be established for APIs in accordance with accepted standards and consistent with the manufacturing process. The specifications should include a control of the impurities e.g. organic impurities, inorganic impurities, and residual solvents). If the API needs to be of a specified microbiological purity, appropriate action limits for total microbial counts, objectionable organisms, and endotoxins may need to be established and met.
11.15 Laboratory controls should be followed and documented at the time of performance. Any deviation from the above described procedures should be documented and justified.
11.16 Any out-of-specification result obtained should be investigated and documented according to a procedure. This procedure should require analysis of the data, assessment of whether a significant problem exists, allocation of the tasks for corrective actions and conclusions. Any resampling and/or retesting after OOS results should be performed according to a documented procedure.
11.17 Primary standards should be obtained as appropriate for the manufacture of APIs. The source of each primary standard should be documented. Records should be maintained of each primary standards storage and use in accordance with the supplier's recommendations. Primary reference standards obtained from an officially recognised source need not be tested if stored under conditions consistent with the supplier's recommendations.
11.18 In cases where a primary standard is necessary and one is not available from an officially recognized source, an "in-house primary standard" should be established. This standard may be prepared by independent synthesis or by further purification of existing production material. Appropriate testing should be performed to establish fully the identity and purity. Appropriate documentation of this testing should be maintained.
11.19 Secondary laboratory reference standards should be appropriately prepared, identified, tested, approved, and stored. The suitability of each batch of secondary reference standard should be determined prior to first use by comparing against a primary reference standard. Each batch of secondary reference standard should be periodically requalified in accordance with a written protocol.
11.2 Testing of Intermediates and APIs
11.20 For each batch of intermediate and API, appropriate laboratory tests should be conducted to determine conformance to specifications.
11.21 An impurity profile describing the identified and unidentified impurities present in a typical batch produced by a specific controlled production process should normally be established for each API. The impurity profile includes the identity or some qualitative analytical designation (e.g. retention time), the range of each impurity observed, and classification of each identified impurity (e.g. inorganic, organic, solvent). The impurity profile is normally dependent upon the process and origin of the API. Impurity profiles are normally not necessary for APIs from herbal or animal tissue origin. Biotech considerations are covered in ICH Guideline Q6B.
11.22 The impurity profile should be compared at appropriate intervals against the impurity profile in the regulatory submission or compared against historical data in order to detect changes to the API resulting from modifications in raw materials, equipment operating parameters, or the production process.
11.23 Appropriate microbiological tests should be conducted on each batch of intermediate and API where a defined microbial quality is necessary.
11.3 Validation of Analytical Procedures - see Section 12.
11.4 Certificates of Analysis
11.40 Authentic Certificates of Analysis should be issued for each batch of intermediate or API on request.
11.41 Information on the name of the intermediate or API including its grade, where appropriate, the batch number, the date of release, and the expiry date should be provided on the label and Certificate of Analysis. For intermediates or APIs with a retest date, the retest date should be indicated on the label and/or Certificate of Analysis.
11.42 The Certificate should list each test performed in accordance with compendial or customer requirements, including the acceptance limits, and the numerical results obtained (if test results are numerical).
11.43 Certificates should be dated and signed by authorised personnel of the quality unit(s) and should show the name, address and telephone number of the original manufacturer. In case the analysis has been carried out by a repacker or reprocessor, the Certificate of Analysis should show the name, address and telephone number of the repacker/reprocessor and a reference to the name of the original manufacturer.
11.44 If new Certificates are issued by or on behalf of repackers/reprocessors, agents or brokers, these Certificates should show the name, address and telephone number of the laboratory that performed the analysis. They should also contain a reference to the name and address of the original manufacturer and to the original batch Certificate, a copy of which should be attached.
11.5 Stability Monitoring of APIs
10.52 A documented, on-going, testing program should be designed to monitor the stability characteristics of APIs, and the results should be used to confirm appropriate storage conditions and retest or expiry dates. Where appropriate, these programs should be consistent with the ICH guidelines on stability.
11.51 The test procedures used in stability testing should be validated and be stability indicating.
11.52 Stability samples should be stored in containers that simulate the market container. For example, if the API is marketed in bags within fiber drums, stability samples may be packaged in bags of the same material and in smaller-scale drums of similar or identical material composition to the market drums.
11.53 Normally the first three commercial production batches should be placed on the stability monitoring program to confirm the retest or expiry date. However, where data from previous studies shows that the API is expected to remain stable for at least two years, fewer than three batches may be used.
11.54 Thereafter, at least one batch per year of API manufactured (unless none is produced that year) should be added to the stability monitoring program and tested at least annually to confirm the stability.
11.55 For APIs with short shelf-lives, testing should be done more frequently. For example, for those biotechnological/biologic and other APIs with shelf-lives of one year or less, stability samples should be obtained and should be tested monthly for the first three months, and at three month intervals after that. When data exist that confirm that the stability of the API is not compromised, elimination of specific test intervals (e.g. 9 month testing) may be considered.
11.6 Expiry and Retest Dating
11.60 When an intermediate is intended to be transferred outside the control of the manufacturer's material management system and an expiry or retest date is assigned, supporting stability information should be available (e.g. published data, test results).
11.61 An API expiry or retest date should be based on an evaluation of data derived from stability studies. Common practice is to use a retest date, not an expiration date.
11.62 Preliminary API expiry or retest dates may be based on pilot scale batches if (1) the pilot batches employ a method of manufacture and procedure that simulates the final process to be used on a commercial manufacturing scale; and (2) the quality of the API represents the material to be made on a commercial scale.
11.63 A representative sample should be taken for the purpose of performing a retest.
11.7 Reserve/Retention Samples
11.70 Reserve samples are maintained for the purpose of evaluating the quality of batches of API at a later date, if necessary. The packaging and holding of these samples is for the purpose of potential future evaluation and not for future stability testing purposes.
11.71 Appropriately identified reserve samples of each API batch should be retained for one year after the expiry date of the batch assigned by the manufacturer, or for three years after distribution of the batch, whichever is the longer. For APIs with retest dates, similar reserve samples should be retained for three years after the batch is completely distributed from the manufacturer.
11.72 The reserve sample should be stored under conditions consistent with product labels, in the same packaging system in which the API is stored or in one that is equivalent to or more protective than the marketed packaging system. Sufficient quantities should be retained to conduct at least two full compendial analyses or, when there is no pharmacopeial monograph, two full specification analyses.
12.1 Validation Policy
12.10 The company's overall policy, intentions, and approach to validation, including the validation of production processes, cleaning procedures, analytical methods, in-process control test procedures, computerized systems, and persons responsible for design, review, approval and documentation of each validation phase, should be documented.
12.11 The critical parameters/attributes should normally be identified during the development stage or from historical data, and the ranges necessary for the reproducible operation should be defined. This should include:
- Defining the API in terms of its critical product attributes;
- Identifying process parameters that may affect the critical quality attributes of the API;
- Determining the range for each critical process parameter expected to be used during routine manufacturing and process control.
12.12 Validation should extend to those operations determined to be critical to the quality and purity of the API.
12.2 Validation Documentation
12.20 A written validation protocol should be established that specifies how validation of a particular process will be conducted. The protocol should be reviewed and approved by the quality unit(s) and other designated units.
12.21 The validation protocol should specify critical process steps and acceptance criteria as well as the type of validation to be conducted (e.g. retrospective, prospective, concurrent) and the number of process runs.
12.22 A validation report that cross-references the validation protocol should be prepared, summarising the results obtained, commenting on any deviations observed, and drawing the necessary conclusions, including recommending changes necessary to correct deficiencies.
12.23 Any changes to the plan as defined in the validation protocol should be documented with appropriate justification.
12.30 Before starting process validation activities, appropriate qualification of equipment and ancillary systems should be completed. Qualification is usually carried out by conducting the following activities, individually or combined:
- Design Qualification (DQ) is documented verification that the proposed design of the facilities, equipment, or systems is suitable for the intended purpose.
- Installation Qualification (IQ) is documented verification that the equipment or systems, as installed or modified, comply with the approved design and the manufacturer's recommendations.
- Operational Qualification (OQ) is documented verification that the equipment or systems, as installed or modified, perform as intended throughout the anticipated operating ranges.
- Performance Qualification (PQ) is documented verification that the equipment and ancillary systems, as connected together, can perform effectively and reproducibly based on the approved process method and specifications.
12.4 Approaches to Process Validation
12.40 Process Validation (PV) is the documented evidence that the process, operated within established parameters, can perform effectively and reproducibly to produce an intermediate or API meeting its predetermined specifications and quality attributes.
12.41 There are three approaches to validation. Prospective validation is the preferred approach, but there are exceptions where the other approaches may be used. These approaches and their applicability are listed below.
12.42 Prospective validation should normally be performed for all API processes as defined in 12.12. Results of prospective validation when performed on an API process must be completed at the latest before the commercial distribution of the final drug product manufactured from that API.
12.43 Concurrent validation may be conducted when data from replicate production runs are unavailable because only a limited number of API batches have been produced, API batches are produced infrequently, or API batches are produced by a validated process that has been modified. Prior to the completion of concurrent validation, batches may be released and used in final drug product for commercial distribution based on thorough monitoring and testing of the API batches.
12.44 An exception may be made for retrospective validation for well established processes that have been used without significant changes to API quality due to changes in raw materials, equipment, systems, facilities, or the production process. This validation approach may be used where:
(1) Critical quality attributes and critical process parameters have been identified;
(2) Appropriate in-process acceptance criteria and controls have been established;
(3) There have not been significant process/product failures attributable to
causes other than operator error or equipment failures unrelated to equipment
(4) Impurity profiles have been established for the existing API.
12.45 Batches selected for retrospective validation should be representative of all batches made during the review period, including any batches that failed to meet specifications, and should be sufficient in number to demonstrate process consistency. Additional testing of retained samples may be needed to obtain the necessary amount or type of data to retrospectively validate the process.
12.5 Process Validation Program
12.50 The number of process runs needed for validation should depend on the complexity of the process or the magnitude of the process change being considered. For prospective and concurrent validation, three consecutive successful production batches should be used as a guide, but there may be situations where additional process runs are warranted to prove consistency of the process (e.g., complex API processes or API processes with prolonged completion times). For retrospective validation, generally data from ten to thirty consecutive batches should be examined to assess process consistency, but fewer batches may be examined if justified.
12.51 Critical process parameters should be controlled and monitored during process validation studies. Process parameters unrelated to quality, such as variables controlled to minimize energy consumption or equipment use, need not be included in the process validation.
12.52 Process validation should confirm that the impurity profile for each API is within the limits specified. The impurity profile should be comparable to or better than historical data and, where applicable, the profile determined during process development or for batches used for pivotal clinical and toxicological studies.
12.6 Periodic Review of Validated Systems
12.60 Systems and processes should be periodically evaluated to verify that they are still operating in a valid manner. Where no significant changes have been made to the system or process, a quality review with evidence that the system or process is consistently producing product meeting its specifications fulfils the need for revalidation.
12.7 Cleaning Validation
12.70 Cleaning procedures should normally be validated. In general, cleaning validation should be directed to situations or process steps where contamination or incidental carryover of materials pose the greatest risk to API quality. For example, in early production it may be unnecessary to validate equipment cleaning procedures where residues are removed by subsequent purification steps.
12.71 Validation of cleaning procedures should reflect actual equipment usage patterns. If various APIs or intermediates are manufactured in the same equipment and the equipment is cleaned by the same process, a representative intermediate or API may be selected for cleaning validation. This selection may be based on the solubility and difficulty of cleaning and the calculation of residue limits based on potency, toxicity, and stability.
12.72 The cleaning validation protocol should describe the equipment to be cleaned, procedures, materials, acceptable cleaning levels, parameters to be monitored and controlled, and analytical methods. The protocol should also indicate the type of samples to be obtained and how they are collected and labelled.
12.73 Sampling should include swabbing, rinsing, or alternative methods (e.g., direct extraction), as appropriate, to detect both insoluble and soluble residues. The sampling methods used should be capable of quantitatively measuring levels of residues remaining on the equipment surfaces after cleaning. Swab sampling may be impractical when product contact surfaces are not easily accessible due to equipment design and/or process limitations (e.g., inner surfaces of hoses, transfer pipes, reactor tanks with small ports or handling toxic materials, and small intricate equipment such as micronizers and microfluidizers).
12.74 Validated analytical methods having sensitivity to detect residues or contaminants should be used. The detection limit for each analytical method should be sufficiently sensitive to detect the established acceptable level of the residue or contaminant. The method's attainable recovery level should be established. Residue limits should be practical, achievable, verifiable and based on the most deleterious residue. Limits may be established based on the minimum known pharmacological, toxicological, or physiological activity of the API or its most deleterious component.
12.75 Equipment cleaning/sanitization studies should address microbiological and endotoxin contamination for those processes where there is a need to reduce total microbiological count or endotoxins in the API, or other processes where such contamination may be of concern (e.g., non-sterile APIs used to manufacture sterile products).
12.76 Cleaning procedures should be monitored at appropriate intervals after validation to ensure that these procedures are effective when used during routine production. Equipment cleanliness may be monitored by analytical testing and visual examination, where feasible. Visual inspection may allow detection of gross contamination concentrated in small areas that could go undetected by sampling and/or analysis.
12.8 Validation of Analytical Methods
12.80 Analytical methods should be validated unless the method employed is included in the current edition of an official pharmacopoeia or other recognised standard references. The suitability of all testing methods used should nonetheless be verified under actual conditions of use and documented.
12.81 Methods should be validated to include consideration of characteristics included within the ICH guidelines on validation of analytical methods. The degree of analytical validation performed should reflect the purpose of the analysis and the stage of the API process.
12.82 Appropriate qualification of analytical equipment should be considered before starting validation of analytical methods.
12.83 Complete records should be maintained of any modification of a validated analytical method. Such records should include the reason for the modification and appropriate data to verify that the modification produces results that are as accurate and reliable as the established method.
13 Change Control
13.10 A formal change control system should be established to evaluate all changes that may affect the production and control of the intermediate or API .
13.11 Written procedures should provide for the identification, documentation, appropriate review, and approval of changes in raw materials, specifications, analytical methods, facilities, support systems, equipment (including computer hardware), processing steps, labelling and packaging materials, and computer software.
13.12 Any proposals for GMP relevant changes should be drafted, reviewed, and approved by the appropriate organisational units, and reviewed and approved by the quality unit(s).
13.13 The potential impact of the proposed change on the
quality of the intermediate or API should be evaluated. A classification procedure may
help in determining the level of testing, validation, and documentation needed to justify
changes to a validated process. Changes may be classified (e.g. as minor or major)
depending on the nature and extent of the changes, and the effects these changes may
13.14 When implementing approved changes, measures should be taken to ensure that all documents affected by the changes are revised.
13.15 After the change has been implemented, there should be an evaluation of the first batches produced or tested under the change.
13.16 The potential effects of critical process changes upon established retest or expiry dates should be evaluated. If necessary, samples of the intermediate or API produced by the modified process may be placed on an accelerated stability program and/or may be added to the stability monitoring program.
13.17 Current dosage form manufacturers should be notified of changes from established production and process control procedures which can impact the quality of the API.
14 Rejection and Re-Use of Materials
14.10 Intermediates and APIs failing to meet established specifications should be identified as such and quarantined. These intermediates or APIs can be reprocessed or reworked as described below. The final disposition of rejected materials should be recorded.
14.20 Introducing an intermediate or API, including one which does not conform to standards or specifications, back into the process and reprocessing by repeating a crystallization step or other appropriate chemical or physical manipulation steps (e.g., distillation, filtration, chromatography, milling) that are part of the established manufacturing process is generally acceptable. However, if such reprocessing is used for a majority of batches, such reprocessing should be included as part of the standard manufacturing process.
14.21 Continuation of a chemical reaction after an in-process control test shows the reaction to be incomplete is considered to be part of the normal process. This is not considered to be reprocessing.
14.22 Introducing unreacted material back into a process and repeating a chemical reaction is considered to be reprocessing unless it is part of the established process. Such reprocessing should be preceded by careful evaluation to ensure that the quality of the intermediate or API is not adversely impacted due to the potential formation of by-products and over reacted materials.
14.30 Before a decision is taken to rework batches that do not conform to established standards or specifications, an investigation into the reason for non-conformance should be performed.
14.31 Batches that have been reworked should be subjected to appropriate evaluation, testing, stability testing if warranted, and documentation to show that the reworked product is of equivalent quality to that produced by the original process. Concurrent validation is often the appropriate validation approach for rework procedures. This allows a protocol to define the rework procedure, how it will be carried out, and the expected results. If there is only one batch to be reworked, then an interim report can be written and the batch released once it is found to be acceptable.
14.32 Procedures should provide for comparing the impurity profile of each reworked batch against batches manufactured by the established process. Where routine analytical methods are inadequate to characterize the reworked batch, additional methods should be used.
14.4 Recovery of Materials and Solvents
14.40 Recovery (e.g. from mother liquor or filtrates) of reactants, intermediates, or the API is acceptable, provided that approved procedures exist for the recovery and that the recovered materials meet specifications suitable for their intended use.
14.41 Solvents may be recovered and reused in the same processes or in different processes, provided that the recovery procedures are controlled and monitored to ensure that solvents meet appropriate standards before reuse or co-mingling with other approved materials.
14.42 Fresh and recovered solvents and reagents may be combined if adequate testing has shown their suitability for all manufacturing processes in which they may be used.
14.43 The use of recovered solvents, mother liquors, and other recovered materials should be adequately documented.
14.50 Returned intermediates or APIs should be identified as such and quarantined.
14.51 If the conditions under which returned intermediates or APIs have been stored or shipped before or during their return or the condition of their containers casts doubt on their quality, the returned intermediates or APIs should be reprocessed, reworked, or destroyed, as appropriate.
14.52 Records of returned intermediates or APIs should be maintained. For each return, documentation should include:
- Name and address of the consignee
- Intermediate or API, batch number, and quantity returned
- Reason for return
15 Complaints and Recalls
15.10 All quality related complaints, whether received orally or in writing, should be recorded and investigated according to a written procedure.
15.11 Complaint records should include:
- Name and address of complainant;
- Name (and, where appropriate, title) and phone number of person submitting the complaint;
- Complaint nature (including name and batch number of the API);
- Date complaint is received;
- Action initially taken (including dates and identity of person taking the action);
- Follow-up action taken (if necessary);
- Response provided to the originator of complaint (including date response sent); and
- Final decision on intermediate or API batch or lot.
15.12 Records of complaints should be retained in order to evaluate trends, product-related frequencies, and severity with a view to taking additional, and if necessary, immediate corrective action.
15.13 There should be a written procedure that defines the circumstances under which a recall of an intermediate or API should be considered.
15.14 The recall procedure should designate who should be involved in evaluating the information, how a recall should be initiated, who should be informed about the recall, and how the recalled material should be treated.
15.15 In the event of a serious or potentially life-threatening situation, local, national, and/or international authorities should be informed and their advice sought.
16 Contract Manufacturers (including Laboratories)
16.10 All contract manufacturers (including laboratories) should comply with the GMP defined in this Guide. Special consideration should be given to the prevention of cross-contamination and to maintaining traceability.
16.11 Contract manufacturers (including laboratories) should be evaluated by the contract giver to ensure GMP compliance of the specific operations occurring at the contract sites.
16.12 There should be a written and approved contract or formal agreement between the contract giver and the contract acceptor that defines in detail the GMP responsibilities, including the quality measures, of each party.
16.13 The contract should permit the contract giver to audit the contract acceptor's facilities for compliance with GMP.
16.14 Where subcontracting is allowed, the contract acceptor should not pass to a third party any of the work entrusted to him under the contract without the contract giver's prior evaluation and approval of the arrangements.
16.15 Manufacturing and analytical records should be kept at the site where the activity occurs and be readily available.
16.16 Changes in the process, equipment, test methods, specifications, or other contractual requirements should not be made unless the contract giver is informed and approves the changes.
17 Agents, Brokers, Distributors, Repackers, and Relabellers
17.10 Throughout Section 17 the term API refers to both API and intermediate.
17.11 This section applies to any party other than the original manufacturer who may trade and/or take possession, handle, repack, relabel, manipulate, or store an API.
17.12 All agents, brokers, distributors, repackers, and relabellers should comply with GMP as defined in this Guide.
17.2 Traceability of Distributed APIs
17.20 Agents, brokers, distributors, repackers, or relabellers should maintain complete traceability of APIs that they distribute. Documents that should be retained and available include:
- Identity of original manufacturer
- Address of original manufacturer
- Purchase orders
- Bills of lading (transportation documentation)
- Receipt documents
- Name or designation of API
- Manufacturer's batch number
- Transportation and distribution records
- All authentic Certificates of Analysis including those of the original manufacturer
- Retest or expiry date
17.3 Quality Management
17.30 Agents, brokers, distributors, repackers, or relabellers should establish, document and implement an effective system of managing quality as specified in Section 2.
17.4 Repackaging, Relabelling and Holding of APIs
17.40 Repackaging, relabelling and holding of APIs should be performed under appropriate GMP controls, as stipulated in this Guide, to avoid mix-ups and loss of API identity or purity.
17.41 Repackaging should be conducted under appropriate environmental conditions to avoid contamination and cross-contamination.
17.50 Stability studies to justify assigned expiration or retest dates should be conducted if the API is repackaged in a different type of container than that used by the API manufacturer.
17.6 Transfer of Information
17.60 Agents, brokers, distributors, repackers, or relabellers should transfer all quality or regulatory information received from an API manufacturer to the customer, and from the customer to the API manufacturer.
17.61 The agent, broker, distributor, repacker, or relabeller who supplies the API to the customer should provide the name of the original API manufacturer and the batch number(s) supplied.
17.62 The agent should also provide the identity of the original API manufacturer to regulatory authorities upon request. The original manufacturer may respond to the regulatory authority directly or through its authorized agents depending on the legal relationship between the authorized agents and the original API manufacturer. (In this context "authorized" refers to authorized by the manufacturer.)
17.63 The specific guidance for Certificates of Analysis included in Section 11.4 should be met.
17.7 Handling of Complaints and Recalls
17.70 Agents, brokers, distributors, repackers, or relabellers should maintain records of complaints and recalls, as specified in Section 15, for all complaints and recalls that come to their attention.
17.71 If the situation warrants, the agents, brokers, distributors, repackers, or relabellers should review the complaint with the original API manufacturer in order to determine whether any further action, either with other customers who may have received this API or with the regulatory authority, or both, should be initiated. The investigation into the cause for the complaint or recall should be conducted and documented by the appropriate party.
17.72 Where a complaint is referred to the original API manufacturer, the record maintained by the agents, brokers, distributors, repackers, or relabellers should include any response received from the original API manufacturer (including date and information provided).
17.8 Handling of Returns
17.80 Returns should be handled as specified in Section 14.52. The agents, brokers, distributors, repackers, or relabellers should maintain documentation for returned APIs.
18. Specific Guidance for APIs Manufactured by Cell Culture/Fermentation
18.10 Section 18 is intended to address specific controls for APIs or intermediates manufactured by cell culture or fermentation using natural or recombinant organisms which have not been covered adequately in the previous sections. It is not intended to be a stand alone Section. In general, the GMP principles in the other sections of this document apply. Note that the principles of fermentation for "classical" processes for production of small molecules and for processes using recombinant and non-recombinant organisms for production of proteins and/or polypeptides are the same, although the degree of control will vary. Where practical this section will address these differences. In general, the degree of control for biotech processes is greater than that for classical fermentation processes.
18.11 Production of APIs or intermediates from cell culture or fermentation involves biological processes such as cultivation of cells or extraction and purification of material from living organisms. Note that there may be additional process steps, such as physicochemical modification, that are part of the manufacturing process. The raw materials (media, buffer components) used may provide good substrates for microbiological contaminants. Depending on the source, method of preparation, and the intended use of the API or intermediate, control of bioburden, viral contamination, and/or endotoxins during manufacturing and monitoring of the process at appropriate stages may be necessary.
18.12 Appropriate controls need to be in place at all stages of manufacturing to preserve intermediate and/or API quality. While this Guide starts at the cell culture/fermentation step, prior steps (e.g. cell banking) should be performed under appropriate process controls. This Guide covers cell culture/fermentation from the point at which a vial of the cell bank is retrieved for use in manufacturing.
18.13 Appropriate equipment and environmental controls
should be used to minimize contamination. The acceptance criteria for quality of the
environment and the frequency of monitoring depend on the step in production and the
production conditions (open, closed, or contained systems).
18.14 In general, process controls should take into account:
- Maintenance of the Working Cell Bank;
- Proper inoculation and expansion of the culture;
- Control of the critical operating parameters during fermentation/cell culture;
- Monitoring of the process for cell growth, viability (for biotech processes) and productivity;
- Harvest and purification procedures that remove cells, cellular debris and media components while protecting the intermediate or API from contamination, particularly of a microbiological nature and loss of intermediate or API quality;
- Bioburden and endotoxin levels should be monitored at appropriate stages of production; and
- For biotech products, viral safety concerns should be as described in ICH Guideline Q5A Quality of Biotechnological Products: Viral Safety Evaluation of Biotechnology Products Derived from Cell Lines of Human or Animal Origin.
18.15 For biotech products, validation of the removal of media components, host cell proteins, other process-related impurities, product related impurities and contaminants may be necessary.
18.2 Cell Bank Maintenance and Record Keeping
18.20 Access to cell banks should be limited to authorized personnel.
18.21 Cell banks should be maintained under storage conditions designed to maintain viability and prevent contamination
18.22 Records of the use of the vials from the cell banks and storage conditions should be maintained
18.23 Cell banks should be periodically monitored to determine suitability for use. For classical fermentation the usage period of the cell strain is usually defined.
18.24 See ICH Guideline Q5D Quality of Biotechnological Products:Derivation and Characterization of Cell Substrates Used for Production of Biotechnological/Biological Products for a more complete discussion of cell banking.
18.3 Cell Culture/Fermentation
18.30 Where possible, closed or contained systems should be used to permit the aseptic addition of cell substrates, media, buffers and gases. If the inoculation of the initial vessel or subsequent transfers or additions (media, buffers) are performed in open vessels, there should be controls and procedures in place to minimize contamination.
18.31 For biotech processes, manipulations using open vessels should be performed in a biosafety cabinet or similarly controlled environment to prevent contamination.
18.32 Personnel should be appropriately gowned and take special precautions handling the cultures.
18.33 Critical operating parameters, for example temperature, pH, agitation rates, addition of gases, pressure, should be monitored to ensure consistency with the established process. Cell growth, viability (for biotech processes), and productivity should also be monitored. Critical parameters will vary from one process to another, and for classical fermentation certain parameters (cell viability, for example) may not need to be monitored.
18.34 Cell culture and fermentation equipment should be cleaned and sterilized after use when used in the manufacture of biotech products. Fermentation equipment for the "classical fermentation" processes should be cleaned and sanitized as appropriate.
18.35 Culture media should be sterilized before use when necessary to protect the quality of the API.
18.36 There should be appropriate procedures in place to detect contamination and determine the course of action to be taken. This should include procedures to determine the impact of the contamination on the product and those to decontaminate the equipment and return them to a condition to be used in subsequent batches. Foreign organisms observed during fermentation processes should be identified as appropriate and the effect of their presence on product quality should be assessed if necessary. The results of such assessments should be taken into consideration in the disposition of the material produced.
18.37 Records of contamination events should be maintained.
18.38 Shared equipment (multi-product) may require additional cleaning or testing between product campaigns, as appropriate, to minimize cross-contamination of previous activities into subsequent activities.
18.4 Harvesting, Isolation and Purification
18.40 Harvesting steps, whether to remove cells from the supernatant (media) or the collection of cellular components after disruption, should be done in equipment and areas designed to minimize contamination, particularly of a microbiological nature.
18.41 Harvest and purification procedures that remove or inactivate the producing organism, cellular debris and media components while minimizing degradation, contamination, and loss of quality, should be adequate to ensure that the intermediate or API is recovered with consistent quality.
18.42 All equipment should be properly cleaned/sanitized after use. Multiple successive batching without cleaning may be utilized if intermediate or API quality is not compromised.
18.43 If open systems are used, purification may need to be done under controlled environmental conditions appropriate for the preservation of product quality. For biotech products this is normally achieved in areas using HEPA filtered air.
18. 44 Additional purification controls, such as dedicated chromatography resins or additional testing, may be necessary if equipment is to be used for multiple products.
18.5 Viral removal /inactivation steps (biotech products only)
18.50 See the ICH Guideline ICH Guideline Q5A Quality of Biotechnological Products: Viral Safety Evaluation of Biotechnology Products Derived from Cell Lines of Human or Animal Origin for more specific information.
18.51 Viral removal and viral inactivation steps are critical processing steps for some biotech processes and should be performed within their validated parameters.
18.52 Appropriate precautions should be taken to prevent potential viral contamination from pre- to post-viral removal/inactivation steps. Therefore, open processing should be performed in separate areas with separate air handling units.
18.53 Separate equipment is normally used for different purification steps. However, if the same equipment is to be used, the respective equipment should be appropriately cleaned and sanitized before reuse. Appropriate precautions should be taken to prevent potential virus carry-over (e.g. through equipment or environment) from previous steps.
19 APIs for Use in Clinical Trials
19.10 Not all the controls in the previous sections of this Guide are appropriate for the manufacture of a new API for investigational use during its development. Section 19 provides specific guidance unique to these circumstances.
19.11 The controls used in the manufacture of APIs for use in clinical trials should be consistent with the stage of development of the drug product incorporating the API. Process and test procedures should be flexible to provide for changes as knowledge of the process increases and clinical testing of a drug product progresses from pre-clinical stages through clinical stages. Once drug development reaches the stage where the API is produced for use in drug products intended for clinical trials, manufacturers should ensure that APIs are manufactured in suitable facilities using appropriate production and control procedures to ensure the quality of the API.
19.20 Appropriate GMP concepts should be applied in the production of APIs for use in clinical trials with a suitable mechanism of approval of each batch.
19.21 A quality unit(s) independent from production should be established for the approval or rejection of each batch of API for use in clinical trials.
19.22 Some of the testing functions commonly performed by the quality unit(s) may be performed within other areas.
19.23 Quality measures should include a system for testing of raw materials, packaging materials, intermediates, and APIs.
19.24 Process and quality problems should be evaluated.
19.25 Labelling for APIs intended for use in clinical trials should be appropriately controlled and identified as being for investigational use.
19.3 Equipment and Facilities
19.30 During all phases of clinical development, including the use of small scale facilities or laboratories to manufacture batches of APIs for use in clinical trials, procedures should be in place to ensure that equipment is calibrated, clean and suitable for its intended use.
19.31 Procedures for the use of facilities should ensure that materials are handled in a manner that minimizes the risk of contamination and cross-contamination.
19.4 Control of Raw Materials
19.40 Raw materials used in production of APIs for use in clinical trials should be evaluated by testing, or received with a supplier's analysis and subjected to identity testing. When a material is considered hazardous, a supplier's analysis should suffice.
19.41 In some instances, the suitability of a raw material may be determined before use based on acceptability in small-scale reactions (i.e., use testing) rather than on analytical testing alone.
19.50 The production of APIs for use in clinical trials should be documented in laboratory notebooks, batch records, or other appropriate means. These documents should include information on the use of production materials, equipment, processing, and scientific observations.
19.51 Expected yields may be more variable and less defined than the expected yields used in commercial processes. Investigations into yield variations are not expected.
19.60 Process validation may be inappropriate during clinical API production where a single API batch may be produced or where process changes during development make batch replication difficult or inexact. The combination of controls, calibration, and, where appropriate, equipment qualification provides the assurance during this development phase.
19.61 Process validation should be conducted in accordance with Section 12 when batches are produced for commercial use, even when such batches are produced on a pilot or small scale.
19.70 Although changes are expected during clinical development, as knowledge is gained and the production is scaled up, every change in the production, specifications, or test procedures should be adequately recorded.
19.8 Laboratory Controls
19.80 All analyses performed to evaluate a batch of API for clinical trials should be scientifically sound; these methods may not yet be fully validated.
19.81 A system for retaining reserve samples of all batches should be in place. This system should ensure that a sufficient quantity of each reserve sample is retained for an appropriate length of time after approval, termination, or discontinuation of an application.
19.82 Expiry and retest dating as defined in Section 11.6 applies to existing APIs used in clinical trials. For new APIs, Section 11.6 does not normally apply in early stages of clinical trials.
19.90 A system should be in place to ensure that information gained during the development and the manufacture of APIs for use in clinical trials is documented and available.
19.91 The development and implementation of the analytical methods used to support the release of a batch of API for use in clinical trials should be appropriately documented.
19.92 A system for retaining production and control records should be used. This system should ensure that records are retained for an appropriate length of time after the approval, termination, or discontinuation of an application.
Active Pharmaceutical Ingredient (API) (or Drug Substance)
Any substance or mixture of substances intended to be used in the manufacture of a drug (medicinal) product and that, when used in the production of a drug, becomes an active ingredient of the drug product. Such substances are intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure and function of the body.
API Starting Material
A material used in the production of an API which is incorporated as a significant structural fragment into the structure of the API. An API Starting Material may be an article of commerce, a material purchased from one or more suppliers under contract or commercial agreement, or it may be produced in-house. API Starting Materials are normally of defined chemical properties and structure.
Batch (or Lot)
A specific quantity of material produced in a process or series of processes so that it is expected to be homogeneous within specified limits. In the case of continuous production, a batch may correspond to a defined fraction of the production. The batch size may be defined either by a fixed quantity or the amount produced in a fixed time interval.
Batch Number (or Lot Number)
A unique combination of numbers, letters, and/or symbols which identifies a batch (or lot) and from which the production and distribution history can be determined.
The level and type (e.g. objectionable or not) of micro-organisms which may be present in raw materials, API starting materials, intermediates or APIs. Bioburden should not be considered contamination unless the levels have been exceeded or defined objectionable organisms have been detected.
The demonstration that a particular instrument or device produces results within specified limits by comparison with those produced by a reference or traceable standard over an appropriate range of measurements.
A group of hardware components and associated software, designed and assembled to perform a specific function or group of functions.
A process or operation integrated with a computer system.
The undesired introduction of impurities of a chemical or microbiological nature, or of foreign matter, into or onto a raw material, intermediate, or API during production, sampling, packaging or repackaging, storage or transport.
A company holding an agreement requiring the performance of some aspect of API manufacturing.
A process step, process condition, test requirement, or other relevant parameter or item that must be controlled within predetermined criteria to ensure that the API meets its specification.
Contamination of a material or product with another material or product.
Drug (Medicinal) Product
The dosage form in the final immediate packaging intended for marketing. (Reference Q1A)
See Active Pharmaceutical Ingredient Expiration Date:
Expiration Date : See Expiry Date
Expiry Date (or Expiration Date)
The date placed on the container/labels of an API designating the time during which the API is expected to remain within established shelf life specifications if stored under defined conditions, and after which it should not be used.
Any component present in the intermediate or API that is not the desired entity.
A description of the identified and unidentified impurities present in an API.
In-Process Control (or Process Control)
Checks performed during production in order to monitor and, if necessary, to adjust the process and/or to ensure that the intermediate or API conforms to its specifications.
A material produced during steps of the processing of an API that must undergo further molecular change or purification before it becomes an API. Intermediates may or may not be isolated.
Lot Number see Batch Number
All operations of receipt of materials, production, packaging, repackaging, labelling, relabelling, quality control, release, storage, and distribution of APIs and the related controls.
A general term used to denote raw materials (starting materials, reagents, solvents), process aids, intermediates, APIs and packaging and labelling materials.
The residual liquid which remains after the crystallization or isolation processes. A mother liquor may contain unreacted materials, intermediates, levels of the API and/or impurities. It may be used for further processing.
Any material intended to protect an intermediate or API during storage and transport.
A documented description of the operations to be performed, the precautions to be taken and measures to be applied directly or indirectly related to the manufacture of an intermediate or API.
Materials, excluding solvents, used as an aid in the manufacture of an intermediate or API that do not themselves participate in a chemical or biological reaction (e.g. filter aid, activated carbon, etc).
See In-Process Control
All operations involved in the preparation of an API, from receipt of materials, through processing and packaging, to its completion as a finished API.
Action of proving and documenting that equipment or ancillary systems are properly installed, work correctly, and actually lead to the expected results. Qualification is part of validation, but the individual qualification steps alone do not constitute process validation.
Quality Assurance (QA)
The sum total of the organised arrangements made with the object of ensuring that all APIs are of the quality required for their intended use and that quality systems are maintained.
Quality Control (QC)
Checking or testing that specifications are met.
An organizational unit independent of production which fulfills both Quality Assurance and Quality Control responsibilities. This may be in the form of separate QA and QC units or a single individual (or group), depending upon the size and structure of the organization.
The status of materials isolated physically or by other effective means pending a decision on their subsequent approval or rejection.
A general term used to denote starting materials, reagents, and solvents intended for use in the production of intermediates or APIs.
Reference Standard, Primary
A substance that has been shown by an extensive set of analytical tests to be authentic material that should be of high purity. This standard may be obtained from an officially recognised source or may be prepared by independent synthesis or by further purification of existing production material.
Reference Standard, Secondary
A substance of established quality and purity, as shown by comparison to a primary reference standard, used as a reference standard for routine laboratory analysis.
Introducing an intermediate or API, including one that does not conform to standards or specifications, back into the process and repeating a crystallization step or other appropriate chemical or physical manipulation steps (e.g., distillation, filtration, chromatography, milling) that are part of the established manufacturing process. Continuation of a chemical reaction after an in-process control test shows the reaction to be incomplete is considered to be part of the normal process, and not reprocessing.
The date when a material should be re-examined to ensure that it is still suitable for use.
Subjecting an intermediate or API that does not conform to standards or specifications to one or more processing steps that are different from the established manufacturing process so that its quality may be made acceptable (e.g., recrystallizing with a different solvent).
See definition for signed
The record of the individual who performed a particular action or review. This record may be initials, full handwritten signature, personal seal, or authenticated and secure electronic signature.
An inorganic or organic liquid used as a vehicle for the preparation of solutions or suspensions in the manufacture of an intermediate or API .
A list of tests, references to analytical procedures, and appropriate acceptance criteria that are numerical limits, ranges, or other criteria for the test described. It establishes the set of criteria to which a material should conform to be considered acceptable for its intended use. "Conformance to specification" means that the material, when tested according to the listed analytical procedures, will meet the listed acceptance criteria.
A documented program that provides a high degree of assurance that a specific process, method, or system will consistently produce a result meeting pre-determined acceptance criteria.
A written plan stating how validation will be conducted and defining acceptance criteria. For example, the protocol for a manufacturing process identifies processing equipment, critical process parameters/operating ranges, product characteristics, sampling, test data to be collected, number of validation runs, and acceptable test results.
The quantity of material or the percentage of theoretical yield anticipated at any appropriate phase of production based on previous laboratory, pilot scale, or manufacturing data.
The quantity that would be produced at any appropriate phase of production, based upon the quantity of material to be used, in the absence of any loss or error in actual production.
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FDA/Center for Drug Evaluation and Research