Root Cause Analysis for CAPA & Best Practices - 2017
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Website http://www.compliance4all.com/control/w_product/~product_id=501587LIVE?channel=ourglocal_Dec_2017_SE |
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Category Root Cause Analysis for CAPA, capa system, corrective and preventive action, CAPA tools, Online CAPA Courses, CAPA Specialists Programs, Compliance Specialists
Deadline: December 11, 2017 | Date: December 12, 2017
Venue/Country: Fremont, U.S.A
Updated: 2017-10-31 15:49:07 (GMT+9)
Call For Papers - CFP
Overview:Refund PolicyBy attending this webinar you will learn about the RCA toolbox and how to get permanent resolution to your significant quality problems.Why should you Attend:You will waste precious time and money and still end up with unsatisfactory results. This webinar will give you insights and lessons learned from a certified Master Black Belt and industry expert with over 30 years' experience. Areas Covered in the Session:Build the right teamDevelop a problem statementFailure InvestigationData CollectionWho Will Benefit:Quality EngineersManufacturing EngineersProcess EngineersCompliance SpecialistsAuditorsSpeaker Profile:Susanne Manz MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities.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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