Equipment and Facility Qualification 2017
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Website http://www.compliance4all.com/control/w_product/~product_id=501615LIVE?channel=ourglocal_Dec_2017_SE |
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Category Equipment Qualification, process validation, pharmaceutical validation, process validation training, process validation course, Manufacturing Engineers, Biopharmaceutical industries
Deadline: December 10, 2017 | Date: December 11, 2017
Venue/Country: Fremont, U.S.A
Updated: 2017-10-31 15:48:02 (GMT+9)
Call For Papers - CFP
Overview:This webinar removes that confusion between equipment Qualification, process validation and Facility commissioning.Why should you Attend:The Webinar is designed for Quality and Manufacturing in the Pharmaceutical and Biopharmaceutical industries.Areas Covered in the Session:Quality Risk Management DefinedCompliance Requirements for Quality Risk ManagementThe Quality Risk Management ModelQuality Risk Management Life CycleWho Will Benefit:Quality EngineersManufacturing EngineersLine ManagersSpeaker Profile:Mr. Muchemu , MSc, MBA is the Co-founder and CEO of CGMP University Inc. Training and consulting organization in San Jose, California. Mister Muchemu is an established author of several GMP books. His background is Chemical Engineering. He has worked in the Pharmaceutical, Medical Device and Tissue industries for over fifteen years.Event Fee: One Dial-in One Attendee Price: US$150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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