Preparing for a US FDA CGMP Compliance Audit Under 21 CFR 210, 211 and 820
Website https://www.complianceonline.com/prepare-fda-cgmp-audit-cfr-webinar-training-706513-prdw?channel=Our |
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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.
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