Elements of a Corrective and Preventive Action (CAPA) Program and Uses of CAPA Data
Website http://bit.ly/2p03szK |
Category capa compliance;examples of capa in pharmaceuticals
Deadline: May 22, 2017 | Date: May 22, 2017
Venue/Country: 2754 80th Avenue, New Hyde Park, NY 11040, U.S.A
Updated: 2017-04-21 20:36:38 (GMT+9)
Call For Papers - CFPOverviewYear after year, CAPA is the subsystem cited most frequently during FDA inspections. A 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.Why Should You AttendThis webinar will identify the most common elements identified as deficient by FDA, and provide recommendations for how to provide clear, concise documentation to assure FDA your firm has addressed these in your quality system. This webinar also provides recommended forms to assure that in addition to being able to illustrate compliance; your firm’s CAPA system is useful and meaningful.Areas Covered in this WebinarRegulatory RequirementsFDA QSRISO 13485Elements of a cross-procedural CAPA programApplications of CAPACAPA Data and best practices for its useApplication of risk management to CAPA programFor more detail please click on this below link:http://bit.ly/2p03szKEmail: firstname.lastname@example.orgToll Free: +1-844-746-4244Tel: +1-516-900-5515Fax: +1-516-900-5510
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