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Part of the Medicines and Healthcare products Regulatory Agency (MHRA), CHM was established in October 2005 combining the responsibilities of Medicines Commission and the Committee on Safety of Medicines. CHM's remit includes:
External link:
Commission on Human Medicines (CHM)
United States adopted name (USAN), Economic regulation, Internal communications, Phase II trials, Pharmacy Benefit Manager (PBM), Informed consent document, National Institute for Health and Clinical Excellence (NICE), Generic medicine, e-Detailing, Lobby, Side-effects, Diagnostic trials, New Drug Application (NDA), Advertising, Double-blind trial,
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