Understanding Corrective and Preventive Action, and Elements of a CAPA System - Webinar by GlobalCompliancePanel

  • 02 Sep 2010
  • Webinar

Description

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. This session will discuss the importance, requirements, and elements of a CAPA program, as well as describing the uses of CAPA data. Additionally, the application of risk management to a CAPA program will be reviewed, and a specific risk management system explained. Areas Covered in the Session:

  • QSR and ISO 13485 requirements for CAPA
  • Elements of a cross-procedural CAPA program
  • Applications of CAPA
  • CAPA data and its uses
  • Application of risk management to CAPA program
Who Will Benefit: This webinar will provide valuable assistance to all regulated companies, a CAPA program is a requirement across the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields. The employees who will benefit include:

  • R&D management
  • Regulatory management
  • QA management
  • Consultants
  • Quality system auditors

Past Events

Important

Please, check "Understanding Corrective and Preventive Action, and Elements of a CAPA System - Webinar by GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Innovations, Legal, Quality assurance
Health & Medicine: Medical device, Pharma

Other Events with Similar Categories

Other Events with Similar Location or Organizer

Featured Conferences & Exhibitions