Analytical Instrument Qualification and System Validation
Website https://www.complianceonline.com/analytical-instrument-qualification-computer-system-validation-semi |
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Deadline: September 07, 2020 | Date: September 17, 2020-September 18, 2020
Venue/Country: Philadelphia, PA, U.S.A
Updated: 2020-05-18 16:21:43 (GMT+9)
Call For Papers - CFP
Analytical equipment should be qualified, and computer systems should be validated to demonstrate suitability for their intended use. To be acceptable to regulatory authorities, electronic records must comply with 21 CFR Part 11, Annex 11 to EU GMPs and more recent data integrity guidance. Recent EU and FDA reports demonstrate that qualification, validation and electronic records are priority areas for inspection. The large number of FDA warning letters and the frequency of EU enforcement action in these areas demonstrate that companies sometimes struggle to understand or implement the regulations.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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