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This presentation covers key FDA initiatives that medical device professionals should be aware of, including inspection trends, device security, Unique Device Identifier (UDI) implementation, and more.
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 a clearer understanding of industry developments in 2016.
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.
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