Understanding the FDA Pathway: Regulatory Basics for Biomedical Device Innovators
Sponsored by Cozen O'Connor
This presentation is designed to help break down the FDA premarket submission process into a practical foundation, explaining fundamentals of device classification, the key premarket submission pathways, and the strategic considerations that can help you avoid common pitfalls and set your product up for success.
Speakers:
Aselle Kurmanova, Member, Cozen O'Connor
Danielle E. Sapega, Member, Cozen O'Connor
FREE!
Online
1/2 Unit CLE
Tuesday, November 11, 2025; 8:30 am to 9:00 am Unsure of the time; check after registration
To register, go to:
https://sites-cozen.vuturevx.com/343/6367/landing-pages/blank.asp?sid=77803dc8-0de7-4152-8855-d6a2c59a4927
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