Things To Do Immediately About Master Validation Plan 2019
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Website https://www.compliance4all.com/control/w_product/~product_id=502268LIVE?channel=ourglocal_Jan_2019_S |
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Category Engineering, Production, Operations, Marketing, Software Validation
Deadline: January 27, 2019 | Date: January 29, 2019
Venue/Country: Online, U.S.A
Updated: 2018-11-07 15:12:39 (GMT+9)
Call For Papers - CFP
Overview:How to develop or improve upon a Master Verification and Validation Plan and System that meets U.S. FDA CGMP, ICH Q-series, and ISO 13485 expectations and requirements.Why should you Attend:The billions of dollars spent by industry annually for V&V are not providing the product safety or efficacy seemingly promised. For most companies, the fixes are not rocket-science, but proper up-front V&V planning and execution, documented in a corporate MVP and implemented by other V&V documents.Areas Covered in the Session:The 11 key documents for software validationIncorporating 21 CFR Part 11 requirementsSuggested "test case" formatsWho Will Benefit:EngineeringProductionOperationsSenior Management in DrugsSpeaker 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: US $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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