| 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 Reaction Terms |
| CRID |
Change Request Identification Number |
| CRO |
Contract Research Organization |
| CTD |
Common Technical Document |
| DIA |
Drug Information Association |
| EEA |
European Economic Area |
| EMA |
European Medicines Agency |
| EU |
European Union |
| EVWEB |
Eudravigilance Web |
| EWG |
Expert Working Group |
| FDA |
Food and Drug Administration (US) |
| 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 of Technical Requirements for
Registration of Pharmaceuticals for Human Use
|
| ICSR |
Individual Case Safety Report |
| IFPMA |
International Federation of Pharmaceutical Manufacturers and Associations |
| J-ART |
Japanese Adverse Reaction Terminology |
| JMO |
Japanese Maintenance Organization |
| JPMA |
Japan Pharmaceutical Manufacturers Association |
| LLT |
Lowest Level Term |
| LOINC |
Logical Observation, Identifiers, Names and Codes |
| MedDRA |
Medical Dictionary for Regulatory Activities |
| MHLW |
Ministry of Health, Labour and Welfare (Japan) |
| MSSO |
Maintenance and Support Services Organization |
| NEC |
Not elsewhere classified |
| NOS |
Not otherwise specified |
| .pdf |
Portable Document File |
| PhRMA |
Pharmaceutical Research and Manufacturers of America |
| PT |
Preferred Term |
| SMQ |
Standardised MedDRA Query |
| SOC |
System Organ Class |
| WHO |
World Health Organization |
| WHO-ART |
World Health Organization Adverse Reaction Terminology |
