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    HEALTHCARE TRAINING 2021 - 6-Hour Virtual Seminar - Batch Record Review and Product Release

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    Deadline: February 26, 2021 | Date: February 26, 2021

    Venue/Country: Online event, U.S.A

    Updated: 2021-01-06 23:36:02 (GMT+9)

    Call For Papers - CFP

    Most Regulatory Agencies require firms to have written procedures in place to document production and process controls, better known as batch records. Additionally, there must be written procedures for a batch record review process that demonstrate compliance.

    A strong batch record review system is essential in order to properly document all critical processing parameters that go along with the production and manufacture of pharmaceuticals, biologics, medical devices, etc.

    This webinar will analyze each of these necessary elements of the batch record review process.

    Why you should attend

    Recognize regulatory requirements for batch records and batch record review

    Discover the essentials of batch record reviewer qualifications and training

    Establish a working relationship between production and quality reviewers

    What to do when a batch fails to meet specifications (discrepancies and deviations)

    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.