RAC Pharmaceuticals EU Regulations Complete Test 2024.
ADR - CORRECT ANSWER Adverse Drug Reaction
AESGP - CORRECT ANSWER Association of the European Self-medication Industry
AIFA - CORRECT ANSWER Italian Medicines Agency
ATMP - CORRECT ANSWER Advanced Therapy Medicinal Products
CA - CORRECT ANSWER Competent Authority
CAT - CORRECT ANSWER Committee on Advanced Therapies
CD-P-PH/ PHO - CORRECT ANSWER European Committee on Pharmaceuticals and Pharmaceutical Care
CEN - CORRECT ANSWER European Committee for Standardization
CHMP - CORRECT ANSWER Committee for Medicinal Products for Human Use
CMD(h) - CORRECT ANSWER Coordination Group for Mutual Recognition and Decentralised Procedures for human medicines
CMS - CORRECT ANSWER Concerned Member State
COMP - CORRECT ANSWER Committee on Orphan Medicinal Products CP - CORRECT ANSWER Centralized Procedure
CTA - CORRECT ANSWER Clinical Trial Application
CTD - CORRECT ANSWER Common Technical Document
CTFG - CORRECT ANSWER Clinical Trials Facilitation Group
CVMP - CORRECT ANSWER Committee for Veterinary Medicinal Products
DAR - CORRECT ANSWER Draft Assessment Report
DCP - CORRECT ANSWER Decentralized Procedure
DG - CORRECT ANSWER Directorate Generals
DLP - CORRECT ANSWER Data Lock Point
DSUR - CORRECT ANSWER Development Safety Update Report
DTCA - CORRECT ANSWER Direct To Consumer Advertising
EC - CORRECT ANSWER European Commission
EC-REP or AR - CORRECT ANSWER European Authorized Representative
EDQM - CORRECT ANSWER European Directorate for the Quality of Medicines
ADR - CORRECT ANSWER Adverse Drug Reaction
AESGP - CORRECT ANSWER Association of the European Self-medication Industry
AIFA - CORRECT ANSWER Italian Medicines Agency
ATMP - CORRECT ANSWER Advanced Therapy Medicinal Products
CA - CORRECT ANSWER Competent Authority
CAT - CORRECT ANSWER Committee on Advanced Therapies
CD-P-PH/ PHO - CORRECT ANSWER European Committee on Pharmaceuticals and Pharmaceutical Care
CEN - CORRECT ANSWER European Committee for Standardization
CHMP - CORRECT ANSWER Committee for Medicinal Products for Human Use
CMD(h) - CORRECT ANSWER Coordination Group for Mutual Recognition and Decentralised Procedures for human medicines
CMS - CORRECT ANSWER Concerned Member State
COMP - CORRECT ANSWER Committee on Orphan Medicinal Products CP - CORRECT ANSWER Centralized Procedure
CTA - CORRECT ANSWER Clinical Trial Application
CTD - CORRECT ANSWER Common Technical Document
CTFG - CORRECT ANSWER Clinical Trials Facilitation Group
CVMP - CORRECT ANSWER Committee for Veterinary Medicinal Products
DAR - CORRECT ANSWER Draft Assessment Report
DCP - CORRECT ANSWER Decentralized Procedure
DG - CORRECT ANSWER Directorate Generals
DLP - CORRECT ANSWER Data Lock Point
DSUR - CORRECT ANSWER Development Safety Update Report
DTCA - CORRECT ANSWER Direct To Consumer Advertising
EC - CORRECT ANSWER European Commission
EC-REP or AR - CORRECT ANSWER European Authorized Representative
EDQM - CORRECT ANSWER European Directorate for the Quality of Medicines
