Jullien L
Regulatory Affairs and Quality
PROJECT TEAM
Acticor
France
Biography
PharmD., Master of International Development and Registration of Drugs. Laurie Jullien started at Genentech (USA) in Product Drug Development and was appointed Regulatory Affairs Labelling Manager at Roche (UK). She is in charge of the regulatory and quality strategy for the development of ACT017, the IMPD dossier and the clinical trial authorisation requests for phase 1 and 2.
Research Interest
Drug Development
