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    FDA’s Expectations from Supplier Management for GMP: Quality Agreements and More

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    Website https://www.complianceonline.com/fda-expectations-from-supplier-management-for-gmp-quality-agreement | Edit Freely

    Category

    Deadline: October 18, 2020 | Date: October 28, 2020

    Venue/Country: U.S.A

    Updated: 2020-09-29 16:07:38 (GMT+9)

    Call For Papers - CFP

    The FDA requires that manufacturers of pharmaceutical products have a documented process to assess its suppliers and contract manufacturers, that they have implemented that process, and that the process is effective. This training program will explore how having an effective supplier relationship management program will result in streamlining the supply chain, ensuring a more consistent level of quality components, materials and components, and be more cost effective to the manufacturer.

    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.