4-Hr Virtual Training: How to Respond to an FDA Investigation
Website https://www.complianceonline.com/how-to-respond-to-an-fda-investigation-preparing-for-fda-audits-res |
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Deadline: December 04, 2019 | Date: December 04, 2019
Venue/Country: U.S.A
Updated: 2019-10-30 19:32:32 (GMT+9)
Call For Papers - CFP
This webinar will illustrate how to respond to an FDA investigation. It could be a 483 observation, a warning letter, or a consent decree, all of which will impact how you carry on your business while under investigation.The course will deconstruct best practices for handling unannounced FDA visits, responding to a 483 or a warning letter, and the effect of an FDA investigation. The program will also discuss basic concepts that should be employed by everyone regulated by the FDA and define processes for preparing for FDA audits.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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