Best Practices in Preparation for an FDA Computer System Audit
Website https://www.complianceonline.com/best-practices-in-fda-computer-system-audit-preparation-webinar-tra |
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Deadline: August 17, 2020 | Date: August 27, 2020
Venue/Country: U.S.A
Updated: 2020-05-19 19:04:52 (GMT+9)
Call For Papers - CFP
FDA requires that all computer systems used to produce, manage and report on “GxP” (GMP, GLC, GCP) related products be validated and maintained in accordance with specific rules. This webinar will help you understand the FDA’s current thinking on computer systems that are validated and subject to inspection and audit. It will also consider areas where FDA will likely focus their effort, including on the higher-risk systems. It will cover areas that will help you to plan for an on-site inspection.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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