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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)
Prescribing information, Drug usage/utilisation review (DUR), Phase I trials, Toxicity, Contraindication, Endpoint, Brief summary, Prevention trials, Fair balance, Phase II trials, Diagnostic trials, Bias, Institutional review board (IRB) - pharmacoeconomics, “P” Medicine, Interventions - clinical,
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