Latest Master Validation Plan - The Unwritten Requirements
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Website https://www.compliance4all.com/control/w_product/~product_id=502519LIVE?channel=ourglocal_Jun_2019_S |
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Category Educational webinars, Healthcare webinars, Biopharmaceutical, Laboratory Managers, pharmaceutical trainings
Deadline: June 16, 2019 | Date: June 18, 2019
Venue/Country: Online, U.S.A
Updated: 2019-04-22 16:16:20 (GMT+9)
Call For Papers - CFP
Overview:FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in many companies. One major failing is lack of sufficient or targeted risk-based company-wide V&V planning.Why should you Attend:Verification and validation requirements have always been part of the US FDA's GMPs.However, with increasing technology, both industry and regulatory agencies expectations have increased.Areas Covered in the Session:The 11 key documents for software validationIncorporating 21 CFR Part 11 requirementsSuggested "test case" formatsWho Will Benefit:SupplementsQARAR&DEngineeringProductionOperationsSpeaker Profile:John E. Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses.Event Fee: One Dial-in One Attendee Price: $290.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: compliance4all14gmail.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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