This webinar will provide a clear, practical overview of how the FDA evaluates whether software functions qualify as medical devices, how to navigate FDA device-related resources, the device risk classification system, and pathways to market.
Is My Software a Medical Device? Understanding FDA Device Regulation Basics
Description:
Webinar Date+Time:
Wednesday, June 25, 20251:00 – 1:30 p.m. EDT
Free Continuing Legal Education Webinar - Register Now!
Credit:
CLE is approved in NY, PA, TX, IL, NV, and CA.
MN CLE has been applied for approval.
You may be able to self-apply for credit in some other states.
Speakers:
- Aselle Kurmanova, Member, Cozen O'Connor
- Danielle E. Sapega, Member, Cozen O'Connor
By:
Cozen O'Connor, established in 1970 and ranked among the top 100 law firms in America, has 750 attorneys who help clients manage risk and make better business decisions.
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