To Facilitate a Closed-Loop Problem Resolution System
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Website http://www.compliance4all.com/control/w_product/~product_id=501648LIVE?channel=ourglocal_Jan_2018_SE |
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Category Root Cause Analysis, CAPA Courses, Device Risk Management, Biologics, Dietary Supplements, Failure Investigation, product risk management
Deadline: January 16, 2018 | Date: January 17, 2018
Venue/Country: Online, U.S.A
Updated: 2017-11-29 15:27:37 (GMT+9)
Call For Papers - CFP
Overview:Defined Failure Investigation and Root Cause Analysis is a major tool in product complaint, non-conformance, and OOS failure investigations.Why should you Attend: Expectations for meaningful CAPA, supported by results-driven Failure Investigation and Root Cause Analysis, that addresses and resolves underlying product problems, are growing among regulatory agencies world-wide.Areas Covered in the Session:Regulatory "Hot Buttons"The 4 Basic Steps to Problem SolvingA Suggested Investigation TemplateID / Document the Problem - CAPA, et alWho Will Benefit:Senior management in Drugs, Devices, Biologics, Dietary 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. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/validations, which have passed FDA audit or submission scrutiny, and described in peer-reviewed technical articles, and workshops, world wide.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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