Latest FDA Changes to the Process Bullet Proof 510k - 2017

Know the differences between the Traditional, Special and Abbreviated

Understand Substantial Equivalence and how it is applied
Who is required to submit the application to FDA

Who Will Benefit:
This course is appropriate to those involved in all aspects of the premarket

notification, i.e., 510(k) process on behalf of medical device and In Vitro

Diagnostic manufacturers.

Speaker Profile:
David R. Dills,Global Regulatory Affairs & Compliance Consultant currently

provides regulatory affairs and compliance consultative services for early-

stage and established Class I/II/III device, IVD, biopharmaceutical,

cosmetics and nutraceutical manufacturers on the global landscape.

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
At a Glance
When 25 July 2017
Where Online
Organizer Netzealous LLC DBA - Compliance4All
Event Type conference
Official Website
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Added by Compliance4all
Added on 15 May 2017
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