Seminar - Online
Vital elements of a robust, "bullet-proof", "closed-loop" Corrective and Preventive Action (CAPA) program include: "Gatekeeper" capture, investigation, verify/validate, monitor, change control methodology, coupled with accurate root cause analysis. Areas Covered in the Session : Regulatory "Hot Buttons" CAPA Background Correction, Corrective Action, Preventive Action Defined Impact Analysis and Response - a Key Component CAPA System Assessment "Bullet-Proof" Data Sources / Metrics Monitor for Effectiveness "Closed-Loop" - Lock In the Change Beyond Regulatory Compliance Who Will Benefit: This 90 minute in-depth webinar will provide valuable assistance to all regulated companies that need to review and modify their company's CAPA system. Its principles apply to personnel / companies in the Medical Devices, Pharmaceutical, Diagnostic, and Biologics fields. The employees who will benefit include: Senior management Middle management R&D Engineering Software QA / RA Manufacturing Operators Consultants cGMP instructors And all personnel involved in verification and/or validation planning, execution and documentation.
Organization: Compliance Trainings (https://compliancetrainings.com )
For more information, please visit: https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1542
Wednesday, June 3, 2015 (13:00 - 14:00)
Mississauga, Ontario 44813, Canada
Contact: Compliance Trainings (suzzane.d@compliancetrainings.com )
Phone: 4169154458
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