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    External GMP Audits for Pharma Companies

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    Website https://www.complianceonline.com/external-gmp-audits-for-pharma-companies-webinar-training-705761-pr | Want to Edit it Edit Freely

    Category

    Deadline: September 13, 2018 | Date: September 13, 2018

    Venue/Country: U.S.A

    Updated: 2018-07-12 22:31:43 (GMT+9)

    Call For Papers - CFP

    Part of any Quality system program is the conducting of External GMP audits. The FDA and other agencies focus on the firms’ External audit programs for suppliers and contractors. An External audit program allows assessment of risk with contractors and suppliers that are used for drug product final release. The program should show how these suppliers and contractors are managed.

    In this session, Mr. Torlini will provide the elements of setting up an External Audit program and the FDA expectations for External Auditing. He will also discuss the need to have R&D and Supply Chain involve with the program. It will also provide guidance on final Quality Agreement that should be in place to capture the responsibilities of both firms.


    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.