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Medical Device Research, Regulations, and Path to Market
Speaker: Kathi Durdon, Executive Director, CNY Biotech Accelerator
This presentation will include an overview of medical device regulations and how risk plays a prominent role in product development, research and regulatory submission and will include an overview of regulatory history, device classification, scientific evidence, premarket submission and postmarket surveillance.

Dec 8, 2022 03:00 PM in Eastern Time (US and Canada)

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