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Healthcare Glossary
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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
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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