Interactive Speaker

Charlène Boumard is Director of Regulatory Strategy, MedTech for Veeva Systems in Europe. With more than 8 years of experience in Regulatory Affairs and Regulatory Compliance/Quality Systems in the industry, she has a deep understanding of the management of international regulatory activities and coordination/collaboration across legal manufacturers and affiliates globally. 

Before joining Veeva, Charlène led a Project Management Office at Abbott Medical, supporting Quality System integrations and harmonization projects across Commercial Affiliates' sites. Charlène represents Veeva in multiple working groups at MedTech Europe to ensure Veeva's products and offerings anticipate industry needs (UDI/EUDAMED, Global International Regulatory Affairs)