In this CAPA training learn how to utilizing multiple data sources to detect actual and potential nonconformities.
Establishing a CAPA system is a requirement of the FDA quality system regulation for medical devices. This Webinar will discuss the key elements of an effective CAPA system, what needs to be addressed in written procedures, and CAPA documentation.
Establishing a CAPA system is a requirement of the FDA quality system regulation for medical devices. This Webinar will discuss the key elements of an effective CAPA system, what needs to be addressed in written procedures, and CAPA documentation.
- What Attendees will Learn
- What are the elements of an effective CAPA system,
- Understand the difference between corrective action and preventive action,
- Strategies to analyze multiple data sources to identify product, process and quality system problems,
- Techniques to establish action limits for CAPA,
- When to use basic quality tools,
- Strategies for achieving regulatory compliance for CAPA documentation.
Who Will Benefit:
- CAPA Managers
- Quality professionals
- Regulatory professionals
- Operations and Engineering personnel
Course Provider
Sue Jacobs,
