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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
Pharmacy Benefit Manager (PBM), Phase II trials, Phase I trials, Institutional review board (IRB) - pharmacoeconomics, Controlled trial, Compassionate use, Generic medicine, Product pipeline, Disease mongering, Line extension, Prompted recall, Efficacy, Clinical, Recruitment status, Adherence,
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