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  • How FDA Trains Its Investigators and Inspectors to Review Sub-Systems for S

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    How FDA Trains Its Investigators and Inspectors to Review Sub-Systems for S

    Wednesday, September 26, 2018 - 9:00 AM
    to Thursday, September 27, 2018 - 5:00 PM

    9:00 AM - 5:00 PM See all dates and Times

    Courtyard Arlington Crystal City/Reagan National A

    https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901747SEMINAR?upcomingevents-sep-seo

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    09/26/2018 09:00 AM 09/27/2018 05:00 PM America/Anguilla How FDA Trains Its Investigators and Inspectors to Review Sub-Systems for S Senior management takes responsibility for Quality and GXP compliance. It is not something delegated to the Quality unit or to the Regulatory Affairs group. Developing and implementing an effective Inspection readiness plan will help ensure better results, as well as a less stressful inspection. Planning strategically ahead will reduce document turn-around time, improve presentation skills from SMEs, and increase inspector confidence in the Quality System. Successfully completing an FDA inspection is critical to cGMP operations and commercial success. Event link : https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901747SEMINAR?upcomingevents-sep-seo Details & Tickets: https://www.upcomingevents.com/philadelphia/events/courtyard-arlington-crystal-cityreagan-national-a/how-fda-trains-its-investigators-and-inspectors-to-review-sub-systems-for-s-35795?ref=uceaddevent Courtyard Arlington Crystal City/Reagan National A, 2899 Jefferson Davis Hwy, Arlington, VA 22202, US, Washington, DC, 22202

    Event Tag

    Seminar / Workshop

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    Business & Networking, Conferences & Tradeshows

    Senior management takes responsibility for Quality and GXP compliance. It is not something delegated to the Quality unit or to the Regulatory Affairs group. Developing and implementing an effective Inspection readiness plan will help ensure better results, as well as a less stressful inspection. Planning strategically ahead will reduce document turn-around time, improve presentation skills from SMEs, and increase inspector confidence in the Quality System. Successfully completing an FDA inspection is critical to cGMP operations and commercial success.

    Event link : https://www.globalcompliancepanel.com/control/globalseminars/~product_id=901747SEMINAR?upcomingevents-sep-seo

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