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Committee for Medicinal Products for Human Use (CHMP)
The Committee is responsible for preparing the European Medicines Agency's (EMA) opinions on all questions concerning medicinal products for human use, in accordance with Regulation (EC) No 726/2004.
See also:
Committee for Medicinal Products for Human Use (CHMP)
Related terms
European Federation of Pharmaceutical Industries (EFPIA), Persistence, British National Formulary (BNF), e-Detailing, Ansoff Matrix, ABPI Code of Practice, Prompted recall, Endpoint, Expanded access, Dose-ranging trial, Defined daily dose (DDD), Commission on Human Medicines (CHM), Detail aid, Off-label use, Concordance programme,
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