Miriam Provost
About Miriam Provost
Vice President of Global Regulatory Affairs
Miriam Provost serves as the Vice President of Global Regulatory Affairs. In this role, she oversees regulatory strategies and compliance for medical devices on an international scale. With her extensive background, she ensures that products align with both local and global regulatory requirements. Her leadership contributes to the successful market entry and sustainability of medical devices worldwide.
Experience in Medical Device Regulatory Affairs
Miriam Provost brings over 24 years of expertise in Medical Device Regulatory Affairs. Her long-standing career has provided her with deep insights into regulatory challenges and solutions. Miriam's experience encompasses strategic planning, compliance enforcement, and regulatory submissions, making her a valuable asset to any medical device company navigating regulatory landscapes.
Work with the Food and Drug Administration
Before her current role, Miriam Provost dedicated 13 years of her career to the Food and Drug Administration (FDA). During her tenure at the FDA, she gained significant experience in regulatory processes, policy development, and compliance monitoring. This foundational experience enriches her perspective and effectiveness in the regulatory affairs sector.
Medical Device Regulatory Consultant
Miriam Provost has also excelled as a medical device regulatory consultant. In this capacity, she advised both large and small medical device companies. She provided strategic guidance and tactical support, helping organizations meet regulatory requirements and bring their products to market. Her consulting work underscores her versatility and deep understanding of the industry.
Education in Chemical Engineering
Miriam Provost's academic background includes a Bachelor's degree in Chemical Engineering from the University of Dayton, as well as M.S. and Ph.D. degrees in Chemical Engineering from the University of Pennsylvania. This strong educational foundation in chemical engineering supports her expertise in medical device regulatory affairs, providing her with a robust technical understanding that informs her professional activities.