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    Preparing for a US FDA CGMP Compliance Audit Under 21 CFR 210, 211 and 820

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    Website https://www.complianceonline.com/prepare-fda-cgmp-audit-cfr-webinar-training-706513-prdw?channel=Our | Edit Freely

    Category

    Deadline: August 15, 2020 | Date: August 25, 2020

    Venue/Country: U.S.A

    Updated: 2020-07-14 20:06:09 (GMT+9)

    Call For Papers - CFP

    Recent US FDA Inspections ("audits") indicate the "c" in CGMP is a moving target – with expectations growing upward! In this webinar, learn how to use the FDA's inspection flow charts and questions, past inspections, and key elements of the CGMPs to prepare for an FDA GMP Compliance Inspection. Recognize that past results are not an accurate of future inspection results. You will learn how to incorporate industry findings into your gap analysis and remediation plan.

    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.