Live webinar A CAPA Primer-Elements of a CAPA Program
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Website https://compliance2go.com/product/?topic=capa-primer-elements-of-a-capa-program |
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Category Biotechnology ; Medical Device ; Pharmaceutical
Deadline: June 17, 2015 | Date: June 18, 2015
Venue/Country: Online, U.S.A
Updated: 2015-05-27 17:07:31 (GMT+9)
Call For Papers - CFP
Date:-Thursday June-18-2015 01:00 PM | 02:00 PM - EDTDESCRIPTIONA robust Corrective and Preventive Action (CAPA) program is of the utmost importance to a medical device manufacturer. A system that identifies and eliminates nonconformances and potential nonconformances enables both regulatory compliance and cost savings. This session will discuss the importance, requirements, and elements of a CAPA program.Areas Covered in the Session:QSR and ISO 13485 requirements for CAPAElements of a cross-procedural CAPA programApplications of CAPACAPA data and its uses Application of risk management to CAPA programWho will benefit:This webinar will provide valuable assistance to all regulated companies, since complaint handling is a regulatory requirement across the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields. The employees who will benefit include:R&D ManagementRegulatory managementQA ManagementConsultantsQuality System AuditorsWebinar Includes:Q/A Session with the Expert to ask your questionPDF print only copy of PowerPoint slides60 Minutes Live PresentationCertificate of Attendance
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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