Enhance your understanding of MDSAP and how it can optimize the market entry process for your products.
Enhance your understanding of MDSAP and how it can optimize the market entry process for your products.
The Medical Device Single Audit Program (MDSAP) streamlines regulatory processes for medical device manufacturers by allowing a single audit to satisfy the requirements of multiple regulatory authorities. In this webinar, you will gain insights into the objectives, benefits, audit process, differences from traditional audits, and preparation steps for manufacturers. With more than 20 years of experience in the regulatory space, our speaker, Dawn Tibodeau, Global Regulatory Affairs Principal at TÜV SÜD, will guide you through these topics and answer your questions in an interactive Q&A session. Don't miss this opportunity to enhance your understanding of MDSAP and how it can optimize the market entry process for your products.
Key topics:
Dawn Tibodeau
Dawn Tibodeau is the Global Regulatory Affairs Principal - MDSAP at TÜV SÜD. With over 20 years at TÜV SÜD, Dawn has held various key roles, including MDSAP Program Specialist and 510(k) 3rd Party Review Program Manager. Her extensive experience and expertise make her an authority in medical device regulations and compliance.
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