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Noemi Manent

European Medicines Agency
Scientific Administrator, Compliance and Inspection
Noémie Manent joined the European Medicines Agency EMA in March 2011 as a Principal Scientific Administrator in the Compliance and Inspection Sector. She is involved in the coordination of EMA Good Clinical Practice (GCP) and pharmacovigilance inspections. She also has a major role in the update of the European Clinical Trial Database (EudraCT) to integrate clinical trial results data to the already established protocol related data and allow for sponsors to publish clinical trial results on the European Clinical Trial Register (www.euclinicaltrialsregister.eu). Currently, she is involved with the implementation of the clinical trial Regulation No. 536/2014 and particularly with the EU portal and database.