A Free Webinar by The FDA Group.
The medical device industry is in a state of transition. Innovation, emerging markets and growing consumer expectations around reliability, security and transparency are prompting regulatory action from the FDA.
This presentation covers key FDA initiatives 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.