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"Welcome in the world of Medical Devices"
The FDA Approval Process for Medical Devices Conference will teach you what is required for 510(k), IDE, PMA, HDE and De Novo applications, how FDA processes premarket submissions, overall FDA medical device regulatory process, and key guidance documents to help ensure a successful process and much more.
Timings9:00 AM - 5:00 PM (General)
Entry FeesPaid Ticket Starts from 1499 GBP View Details
|500 - 1000 |
Category & TypeConference
Medical & Pharma
Editions16 - 17 Sep 2020 Interested
12 - 13 Mar 2019
16 - 17 Oct 2018View More
17 - 18 Apr 2018
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Speakers (past edition)
Afshin HosseinyManaging Director at European Compliance Academy (ECA) Hemel Hempstead, United Kingdom
Visitor Ticket Price
It includes: Gain an Understanding of the FDA, including law, regulations, policies and how the FDA functions/operates, Discover How the 510(k) Process Works, including substantial equivalence determination, format for 510(k) submissions.