Committee for Medicinal Products Human Use (CHMP) - European Medicines Agency
www.ema.europa.eu/en/committees/committee-medicinal-products-human-use-chmp
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The CHMP plays a vital role in the authorisation of medicines in the European Union (EU). In the centralised procedure, the CHMP is responsible for: conducting the initial assessment of EU-wide marketing authorisation applications
In addition, the CHMP and its working parties contribute to the development of medicines and medicine regulation, by: providing scientific advice to companies researching and developing new medicines; preparing scientific guidelines and regulatory guidance to help pharmaceutical companies prepare marketing authorisation applications for human medicines
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