Noemie Manent

Noémie Manent joined the European Medicines Agency in 2011 to coordinate inspections for MAA, she then led the business team to support the submission of summary trial results to the European Clinical Trial Database (EudraCT) and acted as the business lead for the implementation of the Clinical Trial Information System (CTIS), the database required by the Clinical Trial Regulation No. 536/2014. She is currently the Operations Lead for CTIS enabling change management for member states and sponsors Before joining the Agency, Noemie gained more than 15 years experience working in clinical R&D for small and medium enterprises in industry and academia mainly in France and the United Kingdom.