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    Process Validation - Overview of Why and How

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    Website https://www.complianceonline.com/overview-of-process-validation-regulations-and-best-practices-webin | Want to Edit it Edit Freely

    Category

    Deadline: July 24, 2019 | Date: July 24, 2019

    Venue/Country: U.S.A

    Updated: 2019-04-17 19:45:10 (GMT+9)

    Call For Papers - CFP

    Process validation is a requirement but knowing when to validate or revalidate a process is essential. If you do not validate you risk enforcement actions such as fines or recalls, but too much validation is costly in both time and money.

    This webinar will cover the basics of this important topic for those who are new to quality or new to process validation. It will:

    Cover the requirements for process validation from FDA cGMP and ISO 13485.

    Discuss when process validation and revalidation are necessary or desirable.

    Provide an outline of equipment qualification.

    Provide an overview of what is required for process validation.


    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.