This webinar explores the deviation and CAPA processes and best practices for both. It shows how to avoid pitfalls and minimize regulatory scrutiny by having a robust deviation/CAPA system and thorough investigations.
Why Should You Attend:
This webinar will explore and evaluate the deviation and CAPA process. Examples are given to demonstrate the best way to handle deviations and subsequent CAPAs. Attendees will have the opportunity to interact and ask questions about best practices regarding both deviations and the CAPA process. Reasons for having a robust deviation process are given with examples.Areas Covered in the Webinar:
- Typical deviation and CAPA processes within the quality system
- Best practices for the deviation and CAPA processes
- Best practices for documentation
- Tips on how to avoid possible pitfalls with deviations
- Tips on minimizing regulatory scrutiny with deviations
- Examples of good deviation write-ups, investigations and CAPAs
Who Will Benefit:
- Compliance Manager
- Process Engineer
- Production Manager
- Regulatory Manager
- Quality Manager
Course Provider
John R Godshalk,
