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    21 CFR Part 11, FDA's Guidance for Electronic Records and Electronic Signatures

    View: 139

    Website https://www.complianceonline.com/21-cfr-part-11-fda-s-guidance-for-electronic-records-and-electronic | Want to Edit it Edit Freely

    Category

    Deadline: October 24, 2020 | Date: November 03, 2020

    Venue/Country: U.S.A

    Updated: 2020-10-05 15:19:52 (GMT+9)

    Call For Papers - CFP

    The Webinar will focus on the importance of ensuring that electronic record/electronic signature (ER/ES) capability built into FDA-regulated computer systems meets compliance with 21 CFR Part 11. This includes development of a company philosophy and approach, and incorporating it into the overall computer system validation program and plans for individual systems that have this capability.

    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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