Ann-Christine Provoost
Regulatory Affairs Director, Enzymatica AB
Ann-Christine Provoost has over 25 years of experience in leadership and specialist roles within regulatory affairs for medical devices. She has in-depth knowledge of the regulations regarding product development, CE marking, and market access for medical devices across all risk classes. Her experience encompasses both strategic and operational work at the intersection of technology, quality, and regulatory requirements.
Education
Master of Science in Engineering (Materials Science), KTH Royal Institute of Technology, Stockholm.
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