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FDA/ORA
Compliance Policy Guides Manual
2006
Updated: 2008-07-24 |
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Revision/Update History |
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2008 |
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2006 |
2005 |
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1999 |
1998 |
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2008 |
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July 21, 2008
CPG Sec 540.575
Revoked effective 7/15/2008
Revoked by Federal Register notice on 7/18/2008
Compliance Policy Guide Sec. 540.575, Fish
- Fresh and Frozen - Adulteration
Involving Decomposition (CPG 7108.05); (See 73 FR 41361, July
18,2008); CPG 540.575 no longer current.
New Draft "CPG
Sec. 540.370, Fish and Fishery Products -- Decomposition."
The purpose of this Compliance Policy Guide (CPG) is to provide
guidance relating to FDA's direct reference enforcement policy
on decomposition in fish and fishery products.
Revoked effective on 6/6/2008
Revoked by Federal Register notice on 6/6/2008
Sec. 560.700 Processing of Imported Frozen Products of Multiple Sizes (e.g., Shrimp, Prawns, Etc.) (CPG 7119.10)
(See 73 FR 32338 6/6/2008) (CPG Sec. 560.700 is obsolete)
4/11/2008
Final CPG "Guidance for FDA Staff, Sec. 500.500, Guidance Levels for 3-MCPD (3-chloro-1,2-propanediol) in Acid-Hydrolyzed Protein and Asian-Style Sauces." The CPG is available at: http://www.fda.gov/ora/compliance_ref/cpg/cpgfod/cpg500-500.html.
The purpose of this Compliance Policy Guide (CPG) is to provide guidance to help FDA personnel determine whether to take enforcement action based upon the presence of 3-MCPD in acid-HP and Asian-style sauces in interstate commerce or offered for import into the United States.
2/6/2008
New draft CPG "Guidance for FDA Staff, Sec. 555.320, Listeria
monocytogenes."The draft is available at: http://www.fda.gov/ora/compliance_ref/cpg/cpgfod/draft_cpg555-320.html.
The purpose of this draft Compliance Policy Guide is to provide
guidance to FDA Staff on FDA's enforcement policy for Listeria
monocytogenes (L. monocytogenes) in foods.
1/9/2008
New Draft of Revised CPG Section 575.100 - Pesticide Chemical
Residues in Food - Enforcement Criteria. The draft is available
at: http://www.fda.gov/ora/compliance_ref/cpg/cpgfod/draft_cpg575-100.html.
The purpose of this revised draft CPG Sec. 575.100 is to provide guidance for FDA staff regarding FDA's current thinking on its enforcement policy for pesticide chemical residues in food.
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2007 |
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07/13/2007
Compliance
Policy Guide (CPG) entitled, "Sec. 130.300 FDA Access to Results of Quality Assurance Program Audits and Inspections (CPG 7151.02)" was
revised on June 2, 2007, and is now in effect. This CPG was
amended to incorporate the current references and cites to
the Device Quality System Regulation (21 CFR Part 820).
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2006 |
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11/30/2006
Compliance Policy Guide (CPG) 160.900 entitled "Prescription Drug Marketing Act--Pedigree Requirements under 21 CFR Part 203" [PDF Size
42 kb]. This CPG describes how the agency intends to prioritize
its enforcement efforts in the first year after the December
1, 2006, effective date of 21 CFR Sec. 203.3(u) and 203.50. In addition, the
FDA is announcing the availability of a "Guidance for Industry: Prescription Drug Marketing Act Pedigree Requirements Questions and Answers" (PDMA Q & A). The PDMA Q & A guidance is issued in response to the many questions received regarding the Prescription Drug Marketing Act PDMA pedigree requirements. FDA is implementing the PDMA Q&A guidance immediately, because the agency has determined that prior public input is not feasible or appropriate. However, FDA is opening a docket on the PDMA Q & A for interested persons to submit comments and questions. FDA intends to review the comments and questions and to revise the PDMA Q & A
when appropriate. The agency believes that it is important
to maintain FDA's written responses to the significant questions
concerning the PDMA pedigree requirements in a single guidance document
that is periodically updated as the agency receives and responds to
additional questions. We intend to use the following four indicators
to help users of the guidance identify future additions or revisions:
(1) The updated guidance will be identified as a revision of the previously
issued document, (2) the revision date of the guidance will appear on
its cover, (3) the edition number of the guidance will be included in
its title, and (4) questions and answers that have been added to the
guidance, or prior answers that have been in any way modified, will
be identified as such in the body of the guidance. The two guidance
documents explain FDA's current thinking on issues related to the pedigree
requirements of the PDMA.
11/02/2006
Compliance Policy Guide (CPG) entitled, "Sec.
100.550 Status and Responsibilities of Contract Sterilizers Engaged
in the Sterilization of Drugs and Devices (CPG 7150.16)" was
revised on October 3, 2006, and is now in effect. Revisions were
made throughout the CPG, most significantly, to conform to the
device registration regulations. If a contract sterilizer only
distributes sterilized devices to the manufacturer or other registered
firm and does not ship the sterilized devices into commercial distribution,
then it is not required to register with the Center for Devices and Radiological
Health (21 CFR 807.20(c)(2)). Additionally, a contract sterilizer
located in a foreign country is only required to register if it imports,
or offers for import, the sterilized devices into the United States (21
CFR 807.40(a)).
New Guidance That Replaces CPG Sec 110-300,
Compliance Policy Guide Guidance for FDA Staff Registration of
Food Facilities Under the Public Health Security and Bioterrorism
Preparedness and Response Act of 2002"
New Guidance which Replaces CPG Sec. 440.100 Marketed New Drugs Without Approved NDAs or ANDAs (CPG 7132c.02)
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2005 |
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12/12/05
Revised CPG
Sec. 230.150 - Blood Donor Classification Statement, Paid or Volunteer
Donor
Revised CPG
Sec. 300.750 - Class III Devices Subject to 515(b) Requirements
(CPG 7124.18)
Revoked CPG
Sec. 460.700 - Controlled Release Dosage Form Drugs - Rate of
Release of Active Ingredients (CPG 7132a.02)
11/10/2005:
Revised CPG Sec. 110.310 - Prior
Notice of Imported Food Under the Public Health Security and Bioterrorism
Preparedness and Response Act of 2002
08/08/2005:
Revoked by Federal Register notice on 09/24/1998 (63 FR 51074),
CPG Sec. 615.100 Extra-Label
Use of New Animal Drugs in Food-Producing Animals (CPG 7125.06)
05/19/2005
Revised CPG Sec. 315.100 Illegal
Interstate Commercial Shipment of Dentures (CPG 7124.07)
04/25/2005
Revised CPG 100.700 GWQAP
Pre-Award Evaluation - Inadequate Information to Evaluate Prospective
Supplier
04/25/2005
Revised CPG 390.300 Assessment
of Civil Penalties Against Manufacturers and Importers of Electronic
Products
04/13/2005
Revised CPG Sec. 560.400 Imported
Milk and Cream - Federal Import Milk Act CPG 7119.05
03/18/2005
Revised CPG Sec.
300.500 - Reprocessing of Single Use Devices (CPG 7124.16)
03/10/2005
Revised 8 CPGs to make corrections/minor changes: Sec.
390.100;
Sec. 390.400; Sec.
393.100; Sec.
396.300; Sec.
398.100; Sec.
398.325; Sec.
398.425; Sec.
398.700;
03/10/2005
Revoked CPG: Sec.
355.100 - Cellutron Machine
03/08/2005
Revoked 03/08/2005, Compliance Policy Guide, Sec. 160.800 Y2K
Computer Compliance
03/04/2005
Revised CPG Sec. 110.310 - Prior
Notice of Imported Food Under the Public Health Security and Bioterrorism
Preparedness and Response Act of 2002 |
2004 |
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11/16/2004
New CPG Sec. 400.210- Radiofrequency
Identification Feasibility Studies and Pilot Programs
11/03/2004
Revised CPG Sec. 110.300 - Registration
of Food Facilities Under the Public Health Security and Bioterrorism
Preparedness and Response Act of 2002
11/02/2004
Revised CPG Sec. 110.310 - Prior
Notice of Imported Food Under the Public Health Security and Bioterrorism
Preparedness and Response Act of 2002
08/16/2004
Revised CPG Sec. 110.310 -
Prior Notice of Imported Food Under the Public Health Security
and Bioterrorism Preparedness and Response Act of 2002
07/29/2004
Revised CPG Sec. 394.500 - Importation
of Television Products, Microwave Ovens, and Inherent Class I
Laser Products for Investigation and Evaluation
07/29/2004
Replaced/Retitled CPG Sec. 560.750 Guidance
Levels for Radionuclides in Domestic and Imported Foods (CPG
7119.14)
3/12/2004
Revised to update content of August 2000 paper edition:
Sec. 490.100 Process
Validation Requirements for Drug Products and Active Pharmaceutical
Ingredients Subject to Pre-Market Approval CPG 7132c.08
2/9/2004
Edited two pages to conform text (reference) on Internet pages
to August 2000 paper edition CPG Sec. 515.700 Chocolate
& Chocolate Liquor - Adulteration with Insect and Rodent Filth
CPG 7105.11
CPG Sec. 515.775 Cocoa
Powder, Press Cake - Adulteration with Insect and Rodent Filth
CPG 7105.13
Revoked 1/5/2004 Sec.
370.200 RIA Analysis of Hair to Detect the Presence of Drugs
of Abuse CPG 7124.06 |
2003 |
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Issued 12/15/2003
New CPG Sec. 110.300 - "Registration of Food Facilities Under
the Public Health Security and Bioterrorism Preparedness and Response
Act of 2002" is available at: http://www.cfsan.fda.gov/~furls/cpgreg.html. |
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Issued 12/10/2003
Sec. 110.310 - "Prior Notice of Imported Food Under the Public
Health Security and Bioterrorism Preparedness and Response Act
of 2002" is available at: http://www.cfsan.fda.gov/~pn/cpgpn.html |
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Revised 07/08/2003: Sec.
608.400 Compounding of Drugs for Use in Animals (CPG 7125.40)
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Revoked effective 02/19/2003:
Compliance Policy Guide, Enforcement Policy: 21 CFR Part 11; Electronic
Records; Electronic Signatures (CPG 7153.17). See: 68
FR 8775 02/25/2003. |
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2002 |
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Revised 11/14/2002: Sec.
555.600 Filth *from Insects, Rodents, and Other Pests* in Foods
(CPG 7120.18) |
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Revoked effective on 11/12/2002: Sec.
398.475 Minimum X-Ray Field Size for Spot-Film Operation of Fluoroscopic
Systems with Fixed SID and Without Stepless Adjustment of the
Field Size (CPG 7133.17) |
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Revoked effective on 10/07/2002: Sec.
300.700 Direct Reference Authority for Class III Medical Devices
Without a Premarket Notification (510(k)) or an Approved Premarket
Approval Application (PMA) (CPG 7124.30) |
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Revoked effective on 08/07/2002: Sec.
315.200 Status of Dental Supplies such as Denture Cleaners, Adhesives,
Cushions, and Repair Materials as a Device or Cosmetic (CPG 7124.05)
See 67
FR 45129, 07/08/2002 (products are regulated as devices by
regulation) |
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Reissued 05/29/2002: Sec.
460.200 Pharmacy Compounding |
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Revoked 06/20/2002: Sec.
391.100 Advertisement Literature for High-Intensity Mercury Vapor
Discharge Lamps (CPG 7133.13) |
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Revoked 06/20/2002: Sec.
396.100 Applicability of the Sunlamp Performance Standard To UVA
Tanning Products (CPG 7133.16) |
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Corrected 05/16/2002: Sec
575.100 Pesticide Residues...Heptachlor table |
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New 05/16/2002:
Sec. 230.150 Blood Donor
Classification Statement, Paid or Volunteer Donor (Issued 05/07/2002) |
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Revised as Draft Mar 29, 2002: Sec.
345.100 Male Condom Defects (CPG 7124.21) |
2001 |
Top |
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Revised as Draft Dec 18, 2001 - Sec. 555.600 Filth *from Insects, Rodents,
and Other Pests* in Foods (CPG 7120.18) [Final 11/14/2002] |
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New: Oct., 2001 - Sec.
510.150 Apple Juice, Apple Juice Concentrates, and Apple Juice
Products - Adulteration with Patulin |
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Reformat: Oct., 2001 - Sec.
570.425 Tree Nuts - Adulteration Involving Rejects (Insect Infestation,
Moldy, Rancid, Otherwise Decomposed, Blanks, and Shriveled) (CPG
7112.05) |
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Final: April 2001 - Sec.
615.115 Extra-Label Use of Medicated Feeds for Minor Species
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New: April 2001
- Sec. 555.250 Statement
of Policy for Labeling and Preventing Cross-contact of Common
Food Allergens |
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Reformat: March, 2001 - Sec.
220.100 Interstate Shipment of Biological Products for Use in
Medical Emergencies (CPG 7134.11) |
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Reformat: March, 2001 - Sec.
270.100 Final Container Labels - Allergenic Extracts Containing
Glycerin; Reporting Changes (CPG 7134.06) |
2000 |
Top |
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Draft CPG - December 2000, Sec.230.150
Blood Donor Incentives |
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Revised 08/10/2000, Sec.540.650 Uneviscerated
Fish Products that are Salt-cured, Dried, or Smoked (CPG 7108.17)
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New 06/29/2000, Sec. 100.950 International
Partnership Agreements for Compliance Activities - Agreements
among the USFDA, Foreign Government Agencies, and Foreign or Domestic
Trade Associations and/or Other Organizations |
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Revised 08/17/2000, Sec. 230.110 Registration of Blood Banks and Other Firms
Collecting, Manufacturing, Preparing or Processing Human Blood
or Blood Products (CPG 7134.01) |
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New 08/14/2000, Sec. 280.100 Stability
Requirements for Licensed In Vitro Diagnostic Products. |
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New 08/14/2000, Sec. 280.110
Microbiological Control Requirements in Licensed Anti-Human Globulin
and Blood Grouping Reagents |
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Revised 08/10/2000 Sec. 540.650
Uneviscerated Fish Products that are Salt-cured, Dried, or Smoked
(CPG 7108.17) |
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Revised 05/01/2000, Sec. 651.100 Ethylenediamine
Dihydroiodide (EDDI) (CPG 7125.18) |
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Revised 04/14/2000, Sec. 110.100 Certification
for Exports (CPG 7150.01) |
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Deleted 03/28/2000, Sec. 215.100 IND
Filings: Completion of Applicable... |
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Reissued 03/22/2000, Sec. 257.100
Deferral of Source Plasma Donors Due to Red Cell Loss During Collection
of Source Plasma by Automated Plasmapheresis |
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New 03/06/2000, Sec. 252.110 Volume
Limits for Automated Collection of Source Plasma |
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Deleted (Revoked) 01/24/2000, Sec. 305.100 Acupuncture
Devices and Accessories (CPG 7124.11) |
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1999 |
Top |
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Draft CPG 08/04/1999, Sec. 615.115 Use
of Medicated Feeds for Minor Species |
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New 07/09/1999, Sec. 230.140 Evaluation
and Processing Post Donation Information Reports |
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New 05/13/1999, Sec. 160.850 Enforcement Policy:
21 CFR Part 11; Electronic Records;
Electronic Signatures (CPG 7153.17) |
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New 04/26/1999, Sec. 160.800 Y2K
Computer Compliance |
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New 03/23/1999, Sec. 555.425
Foods, Adulteration Involving Hard or Sharp Foreign Objects
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Deleted 01/8/1999, Sec. 460.200 Manufacture,
Distribution, and Promotion of Adulterated, Misbranded, or Unapproved
New Drugs for Human Use by State-Licensed Pharmacies (CPG 7132.16)
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1998 |
Top |
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Revised 11/13/98, Revised Sec. 675.400 Rendered
Animal Feed Ingredients (CPG 7126.24) |
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New 12/21/98, New Sec. 257.100
Deferral of Source Plasma Donors Due To Red Cell Loss During Collection
of Source Plasma by Automated Plasmapheresis |
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*Material between asterisks was changed |
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