The Indiana Medical Device Manufacturers Council (IMDMC) is hosting a workshop on April 21st targeted for those new to the medical device industry or for those looking for a regulatory refresher. There will be multiple presentations including one from Gretchen Bowker COO & RAC, FRAPS, on, Pathways to Market – 510(K) Requirements at 10:15am. The workshop provides a background in FDA regulations of medical devices.
What: A workshop exploring FDA regulations of medical devices and pathways to market.
When: Thursday, April 21st, 2016, 8:00 AM to 5:00 PM EDT
Where: The Montage – 8580 Allison Pointe Boulevard, Indianapolis, IN 46250
New to the medical device industry and want to learn more about the FDA regulations? Register here today! (Lunch will be provided.)
Click here to learn more about the workshop and to register for both workshops, REG 101 & 102. We hope to see you on April 21st!