Validation Master Plan - The Unwritten Requirements
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Deadline: November 20, 2019 | Date: November 20, 2019
Venue/Country: U.S.A
Updated: 2019-07-05 21:07:05 (GMT+9)
Call For Papers - CFP
This 60-minute session on master verification and validation planning will discuss the major cGMP deficiencies and "must have" elements from the U.S. FDA cGMP, ICH Q9 and ISO 14971 for hazard analysis and product risk management, and show how you can integrate these into a company's quality management system.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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