Investigation and Root Cause Analysis to Meet FDA Expectations
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Website https://www.compliance4all.com/control/w_product/~product_id=502546LIVE?channel=ourglocal_Jun_2019_S |
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Category Educational webinars, Healthcare webinars, Biopharmaceutical, Laboratory Managers, pharmaceutical trainings
Deadline: June 24, 2019 | Date: June 26, 2019
Venue/Country: Online, U.S.A
Updated: 2019-04-22 16:20:08 (GMT+9)
Call For Papers - CFP
Overview:This live interactive presentation will also discuss the regulations associated with the detection, correction and prevention of human errors in GMP manufacturing and laboratory processes.Why should you Attend:We will focus on improved techniques to get to the real cause of the problem. With this information you will be able to develop meaningful CAPAs that have a chance to remedy these problems, the first time.Areas Covered in the Session:How to develop a true CAPA for these problemsDevelop an efficient and effective CAPA system to remedy the ingrained problemsIdentification and prevention of human error during data entryWho Will Benefit:Quality Assurance PersonnelQuality Control PersonnelSupply Chain and Logistics ManagersRegulatory Affairs ProfessionalsSpeaker Profile:Angela Bazigos is the CEO of Touchstone Technologies Inc. She has degrees in Microbiology and Computing and 40 years of experience in the Life Sciences, Healthcare & Public Health Services.Event Fee: One Dial-in One Attendee Price: $150.00Contact 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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