FDA Logo links to FDA home page
Center for Drug Evaluation and Research, U.S. Food and Drug AdministrationU.S. Food and Drug AdministrationCenter for Drug Evaluation and Research
  HHS Logo links to Department of Health and Human Services website

FDA Home Page | CDER Home Page | CDER Site Info | Contact CDER | What's New @ CDER

horizonal rule
CDER Home About CDER Drug Information Regulatory Guidance CDER Calendar Specific Audiences CDER Archives
 
Powered by Google
 

Data Standards Manual

The FDA Data Standards Manual (DSM) is a compilation of standardized nomenclature monographs that have been reviewed and approved by the FDA Data Standards Council through their Vocabulary Standards Work Group (VSWG) and through CDER Nomenclature Standards Committee (NSC). These nomenclature standards are considered binding upon all new automated databases, and upon all existing automated databases when undergoing a major redesign.

DSM monographs have been jointly developed by several FDA organizational components after a vetting by subject matter experts. DSM monographs may have been derived either wholly or in part from other nomenclature standards settings bodies, as well, such as the American Hospital Formulary Service (AHFS), the American Society for Testing and Materials (ASTM), the Central Intelligence Agency, the Chemical Abstracts Service (CAS), the Clinical Data Interchange Standards Consortium (CDISC), the Consolidated Health Informatics initiative (CHI), the Department of Veterans Affairs, Federal Medical Terminologies (FMT), Health Level Seven (HL7), the Healthcare Information Technology Standards Panel (HITSP), the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH), the International Organization for Standardization (ISO), the National Institutes of Standards and Technology (NIST), the United States Adopted Names Council (USAN), the United States Census Bureau, the United States Pharmacopeia (USP), and the United States Postal Service.

If you would like to propose a change to one of the DSM monographs, you must first complete a Vocabulary Change Request Form. The VSWG and NSC meets as necessary to discuss proposed changes to the DSM. If you have any questions about the DSM, please contact CAPT William A. Hess at 301-827-7865 or william.hess@fda.hhs.gov.


Authority

 

MaPP 7600.4 Nomenclature Standards Committee

7600.4

SMG 2010.3 FDA Data Standards Council

2010.3

SMG 3060.1 FDA Data Council - Data Standards Program

3060.1


 

Nomenclature Control Policies

Monograph Number


Implementation Policy C-POL-00001
Valid Values Policy C-POL-00002
Center-wide Thesauri,Dictionaries, and Tables Policy C-POL-00003
Metric System and Potency Expression Policy C-POL-00004
Use of Drug Name Terms Policy C-POL-00005

Back to Top


Drug Nomenclature Monographs

Monograph Number


Drug Classification C-DRG-00101
Dosage Form C-DRG-00201
Route of Administration C-DRG-00301
Ingredient Name C-DRG-00401
Proprietary Name C-DRG-00402
Animal Common Names C-DRG-00403
Animal Cell Tissue Fluid Biomolecule C-DRG-00404
Biotechnology Origin C-DRG-00405
Potency C-DRG-00501
Indications C-DRG-00601
Therapeutic Equivalence Code C-DRG-00701
Phase 4 Commitment Category C-DRG-00901
Phase 4 Fulfillment Category C-DRG-00902
Pediatric use Supplement Rule C-DRG-00903
Pediatric Use Supplement Clinical Efficacy Trials Category C-DRG-00904
Pediatric Use Supplement PK/PD Category C-DRG-00905
Pediatric Use Supplement Safety/Adverse Reaction Category C-DRG-00906

Package Type

C-DRG-00907

Pediatric Exclusivity Study Type

C-DRG-00908

Pediatric Exclusivity Study Age Group

C-DRG-00909

Pediatric Exclusivity Study Basis

C-DRG-00910

Pediatric Exclusivity Study Drug List

C-DRG-00911

Geriatric Use Supplement Rule

C-DRG-00913

Geriatric Use Supplement Clinical Efficacy Trials Category

C-DRG-00914

Geriatric Use Supplement PK/PD Category

C-DRG-00915

Geriatric Use Supplement Safety/Adverse Reaction Category

C-DRG-00916

Industry Meeting Type

C-DRG-00917

Industry Meeting Response

C-DRG-00918

PACT Commitment Category

C-DRG-00919

PACT Fulfillment Category

C-DRG-00920

Global Suplement Status

C-DRG-00921

Plant Part C-DRG-00924
SPL Coating C-DRG-0925
SPL Symbol C-DRG-0926
SPL Color C-DRG-0927
SPL Size C-DRG-0928
SPL Shape C-DRG-0929
SPL Score C-DRG-0930
SPL Imprint C-DRG-0931
SPL Image C-DRG-0932
SPL DEA Schedule C-DRG-0933
SPL Flavor New!! C-DRG-0934
Marketing Category C-DRG-0935

Back to Top


General Nomenclature Monographs Monograph Number

Calendar Date - Format 2 C-GEN-00002
Fiscal Year C-GEN-00005
Person Given Name C-GEN-00201
Person Middle Name C-GEN-00202
Person Surname C-GEN-00203
Person Family Rank C-GEN-00204
Sponsor/Applicant Name C-GEN-10201
Telephone Area Code C-GEN-10202
Telephone Country Code C-GEN-10203
Telephone Number, Format 1 C-GEN-10204
Telephone Number, Format 2 C-GEN-10205
Telephone City Code C-GEN-10206
Application Type C-GEN-10207
Application Number C-GEN-10208
Gender C-GEN-10209
Race C-GEN-10210
Marital Status C-GEN-10211
Height C-GEN-10212
Weight C-GEN-10213
Educational Level C-GEN-10301
ECH Document Type C-GEN-10302
FYI Copy Destination C-GEN-10303
Media Type C-GEN-10304
Plant Type C-GEN-10305
DFS Recommendation Code C-GEN-10306

INVAS Volume Type

C-GEN-10307

Back to Top


Geographic Nomenclature Monographs Monograph Number

Countries, Dependencies, and Areas of Special Sovereignty C-GEO-00101
States and Outlying Areas of the United States C-GEO-00204
Street Address C-GEO-00301
City Name C-GEO-00302
State/Foreign Province C-GEO-00303
Country Name C-GEO-00304
District Office Code C-GEO-00305
Division of the World C-GEO-00306

Back to Top


Back to Top     Back to Regulatory Information

Date updated: January 9, 2009

horizonal rule