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    Analytical Instrument Qualification and System Validation

    View: 252

    Website https://www.complianceonline.com/analytical-instrument-qualification-computer-system-validation-semi | Edit Freely

    Category

    Deadline: September 07, 2020 | Date: September 17, 2020-September 18, 2020

    Venue/Country: Philadelphia, PA, U.S.A

    Updated: 2020-04-05 03:33:32 (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.
    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.