The Medical Device Single Audit Program (MDSAP) is an important new global initiative intended to harmonize regulatory efforts around the world.
But despite looming deadlines, comparatively few medical device companies have a meaningful understanding of the advantages (and disadvantages) of pursuing MDSAP certification and how to prepare accordingly.
We're hosting a free webinar offers a clear and practical guide to understanding what the MDSAP is, the kinds of device manufacturers that stand to benefit from it, what to consider before pursuing certification, and how to prepare for the audit sequence.
All registrants and attendees will receive a free recording of the webinar and handy white paper (PDF).
Whether you’re a VP, Director, Regulatory Affairs Manager, Quality Assurance Professional, Consultant, or anyone else involved in ensuring regulatory compliance is maintained, you'll come away with actionable takeaways you can use to make an informed decision about the MDSAP.
Instructor Larry Stevens, RAC, has held almost every field position within FDA during his 21-year career with FDA and has over 18 years of experience in the Medical Device industry rising from an RA Manager to Vice President of RA/QA/Clinical for major class III device manufacturers.