Webinar On FDAs DHF, DMR and DHR will examine the existing and proposed requirements for the U.S. FDA's DHF per the CGMPs, 21 CFR 820.30 (j)

Date : 16th December 2015 to 16th December 2015

Place : United States, New hyde park

Website :https://www.complianceglobal.us/product/700098

Contact Person:Roger Davis

Description:

Webinar On FDAs DHF, DMR and DHR will examine the existing and proposed requirements for the U.S. FDA's DHF per the CGMPs, 21 CFR 820.30 (j)

Webinar On FDAs DHF, DMR and DHR will examine the existing and proposed requirements for the U.S. FDA's DHF per the CGMPs, 21 CFR 820.30 (j) will be held in New hyde park,United States on date 2015-12-16

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Deadline for abstracts/proposals : 16th December 2015

Keynote Speakers : John E. Lincoln, is Principal of J. E. Lincoln and Associates LLC, a consulting company with over 33 years' experience in U.S. FDA regulated industries, 19 of which are as an independent consultant. John has worked with companies from start-up to Fortune 100, in the U.S., Mexico, Canada, France, Germany, Sweden, China and Taiwan.

Conference Highlights :One of our most popular webinars, continuously updated with the latest U.S. FDA and European Union requirements. As U.S. companies go global, they must meet different product design documentation. The Device (21 CFR 820) and Combination Products (21 CFR 4) cGMPs mandate Design Control and the Design History File (DHF). In order to sell globally, the EU's CE-marking documentation is a requirement -- the Technical FiIe or Design Dossier. Currently they serve different purposes, support di

Venue :Online Webinar For more information Email: [email protected] Toll Free: +1-844-746-4244 Tel: +1-516-900-5515

Check the event website for more details.