Understanding good Closed Loop CAPA system - Webinar By GlobalCompliancePanel
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Website http://www.globalcompliancepanel.com |
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Category regulatory compliance training, regulatory compliance, regulatory affair; Regulatory standards; Regulatory Trainings; Regulatory Environment
Deadline: June 09, 2011 | Date: June 09, 2011
Venue/Country: Wilmington | DE, U.S.A
Updated: 2011-06-02 19:40:16 (GMT+9)
Call For Papers - CFP
This webinar will present how organizations can pursue continual improvements and address the concerns of non-conformances and develop corrective/preventive actions to prevent the repetition of these occurrences in the future.Increased regulatory pressures, the latest customer mandates and internal quality initiatives are requiring companies to take a proactive and automated approach to their corrective action process. In addition, regulatory compliance requires organizations to capture all corrective action issues and track their corrective action process to completion.Areas Covered in the Session:Importance of CAPA ProcessRoles within the CAPA ProcessElements of a Closed Loop CAPA processImportance of Risk Analysis ProcessWhat needs to be in place for ComplianceSoftware Solution RequirementsWho Will Benefit:Quality Assurance PersonnelBusiness Process OwnersCompliance PersonnelRegulatory PersonnelInternal AuditorsPrice List:Live : $245.00Corporate live : $995.00Recorded : $295.00
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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