ÂÜÀòÂÒÂ×

Caroline Mandret has extensive experience in regulatory product information systems and pharmacovigilance, starting as a Drug Safety Officer at Bayer in 2007. Caroline later transitioned to Altran as a Consultant before joining Stallergenes Greer in 2010. At Stallergenes Greer, they held roles such as Drug Safety Coordinator, Safety Database Manager, and Manager of Regulatory Product Information Systems/IDMP Project Lead, where they managed regulatory databases, ensured data availability in compliance with IDMP standards, and led various related projects.

Caroline Mandret completed a DU de Pharmacovigilance et sécurité du médicament at Université Paris Cité in 2011. In 2012, they also attended DIA for courses in Electronic reporting of ICSRs and eXtended EV Medicinal Product Dictionary (XEVMPD) in the field of Pharmacovigilance.