Committee for Human Medicinal Products - Strategic Review and Learning Meeting

The Committee for Medicinal Products for Human Use of the European Medicines Agency (EMA) is responsible for the authorisation of medicinal products through the centralised procedure in the European Union. The Strategic Review and Learning Meeting (SRLM) of the CHMP organized by the EU presidency MS aims at providing an opportunity for strategic discussions of the Committee and facilitate the exchange of views, experiences and scientific developments, developing the future work of the Committee.