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    Best Practices in Preparation for an FDA Computer System Audit

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    Website https://www.complianceonline.com/best-practices-in-fda-computer-system-audit-preparation-webinar-tra | Edit Freely

    Category

    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.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.