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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
Core message, McKinsey Seven S's of Management (or 7-S Model), External analysis, Reinforcement advertising, Clinical trial enrolment, Moderator guide, Negative demand, e-Detailing, Random samplings, Institutional review board (IRB) - pharmacoeconomics, Point of sale (POS), Advertising research, Blended e-learning, International nonproprietary name (INN), Collateral PR,
