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    The 6 Most Common Problems in FDA Software Validation and Verification

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    Website https://www.complianceonline.com/6-most-common-problems-in-fda-software-validation-and-verification- | Edit Freely

    Category

    Deadline: October 17, 2020 | Date: October 27, 2020

    Venue/Country: U.S.A

    Updated: 2020-09-29 16:05:44 (GMT+9)

    Call For Papers - CFP

    This webinar describes the validation planning process with particular emphasis on avoiding six common pitfalls. Increased use of software from automated manufacturing and quality systems means increased exposure. Most recalls can be traced back to computerized equipment, exposing the validation process to scrutiny. Corporate uncertainty leads to inaction and “wheel spinning.” Many companies struggle with understanding how to avoid major mistakes when validating software to FDA standards.

    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.