|
ASCII |
American Standard
Code for Information Interchange |
|
BRP |
Blue Ribbon Panel |
| CIOMS |
Council for International Organizations of Medical Sciences |
| COSTART |
Coding Symbols for a Thesaurus of Adverse Reactions Terms |
|
CRID |
Change Request Identification Number |
|
CRO |
Clinical Research Organization |
| CTD |
Common Technical Document |
| DIA |
Drug Information Association |
| EDI |
Electronic Data Interchange |
|
EEA |
European Economic Area |
| EMEA |
European Medicines Agency |
|
EU |
European Union |
|
EVWEB |
Eudravigilance Web |
| EWG |
Expert Working Group |
| FDA |
Food and Drug Administration |
| HARTS |
Hoechst Adverse Reaction Terminology System |
| HLGT |
High Level Group Term |
| HLT |
High Level Term |
| ICD-9 |
International Classification of Diseases - 9th Revision |
| ICD-9-CM |
International Classification of Diseases - 9th Revision
Clinical Modification |
| ICH |
International Conference on Harmonisation |
| ICSR |
Individual Case Study Report |
| IFPMA |
International Federation of Pharmaceutical Manufacturers and
Associations |
| J-ART |
Japanese Adverse Reaction Terminology |
| JMO |
Japanese Maintenance Organization |
| JPMA |
Japanese Pharmaceutical Manufacturer Association |
| LLT |
Lowest Level Term |
| LOINC |
Logical Observation, Identifiers, Names and Codes |
| MedDRA® |
Medical Dictionary for Regulatory Activities |
| MHLW |
Ministry of Health, Labor and Welfare (Japan) |
| MSSO |
Maintenance and Support Services Organization |
| PDF |
Portable Document File |
| PhRMA |
Pharmaceutical Research and Manufacturers of America |
| PT |
Preferred Term |
|
SMQ |
Standardised MedDRA Query |
| SOC |
System Organ Class |
| SSC |
Special Search Category |
| WHO |
World Health Organization |
| WHO-ART |
World Health Organization Adverse Reaction Terminology |
