This training program will provide professionals with essential elements of CAPA investigations to assure compliance with regulatory requirements. The corrective and preventive action (CAPA) program is an essential element of a compliant quality management system, as required by international regulations and voluntary standards. Investigations are the backbone of the CAPA program.
Why Should You Attend:
A central theme in every CAPA investigation is determination of reoccurrence. Reoccurrence of deviations, non-conformances, or incidents may be indicative of inadequate investigations and/or ineffective identification of CAPAs. Tracking and trending is the process by which reoccurrence is determined and adequacy of the CAPA system as a whole is demonstrated. This webinar has been specifically designed to delineate the essential elements of CAPA investigations.Areas Covered in the Webinar:
- International regulatory requirements for CAPA investigations
- Insight into investigator or auditor expectations from CAPA investigations
- Essential elements of CAPA investigations
- Roles and responsibilities for CAPA investigations
Who Will Benefit:
This CAPA investigations webinar will provide professionals from pharmaceutical, biotechnology, medical device and active pharmaceutical ingredient industries with the necessary tools to investigate non-conformances and deviations. It will be of interest to personnel directly involved in completing, reviewing or approving investigations. Expected participation by:- Quality Engineers
- Manufacturing Engineers
- Quality Systems Managers
- Operations Managers
- Regulatory Compliance professionals
- Consultants
Course Provider
Carlos Rodriguez Garcia,
