The Most Serious FDA 483s - How to Avoid Them
Website https://www.complianceonline.com/the-most-serious-fda-483s-how-to-avoid-them-webinar-training-702766 |
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Deadline: March 12, 2019 | Date: March 12, 2019
Venue/Country: U.S.A
Updated: 2019-01-26 18:06:29 (GMT+9)
Call For Papers - CFP
Recent FDA audits indicate a shift in the top serious Form 483 observations.This webinar will evaluate the chief areas of FDA CGMP compliance audits based on recent top 483 findings to see actual and anticipated changes in emphasis, and how to better prepare with a company's internal audit program .This 90-minute session will provide valuable assistance to all regulated companies in evaluating their existing compliance and internal audit emphasis in light of the changed FDA focus based on recent 483 analysis, and their audit "paradigm". Such analysis allows a company to evaluate/ perform a gap analysis, and then put in place the necessary fixes to ensure continuing compliance.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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