European Commission Adopts Two Acts on GMPs for Medicines
By Zachary Brennan -
Published 10 October 2017
Last month, the European Commission adopted two legal acts seeking to improve patient safety through good manufacturing practices (GMP) that ensure the highest quality of medicines for investigational and human use.
Categories: News, Europe, EC, Biologics and biotechnology, Drugs, Manufacturing
Tags: good manufacturing practices, implementing directive, delegated regulation, GMPs for investigational medicines