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    The Most Serious FDA 483s - How to Avoid Them

    View: 118

    Website https://www.complianceonline.com/the-most-serious-fda-483s-how-to-avoid-them-webinar-training-702766 | Want to Edit it Edit Freely

    Category

    Deadline: March 12, 2019 | Date: March 12, 2019

    Venue/Country: U.S.A

    Updated: 2019-02-08 20:11:00 (GMT+9)

    Call For Papers - CFP

    This webinar on avoiding serious FDA 483s will explain FDA's changed audit focus based on recent top 483 findings and provide practical tips on how to better prepare your company's internal audit program to avoid serious Form 483 observations.

    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.