Good Documentation Practice (GDocP) for FDA Regulated Industry
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Deadline: December 16, 2019 | Date: December 16, 2019
Venue/Country: U.S.A
Updated: 2019-11-04 21:27:25 (GMT+9)
Call For Papers - CFP
This good documentation practice webinar will discuss how to secure, manage and govern your documentation in compliance with GxP/GMP requirements and be able to pass quality audit. Also attendees will learn the connection between CxP/GMP and document control, which documents need to be controlled and which are not, what documentation required for QMS, how QA can plays an important role in documentation systems and how change control procedure used in GxP/GMP environment.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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