Compliance Trainings, Online
2015-06-03
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. 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: 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. Price tags: Live Single Live : For One Participant $ 249 Corporate Live : For Max. 10 Participants $ 899 Recording Single REC : For One Participant - Unlimited Access for 6 Months $ 299 For more information and enquiries contact us at Compliance Trainings 5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada Customer Support : #416-915-4458 Email : support@compliancetrainings.com
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