Overview: Manufacturers continue to struggle with CAPA systems as evidenced by FDA Warning Letters which show a large percentage of citations are for inadequate CAPA Systems.
One of the tools that can help assign resources for CAPA to complete actions in a timely manner is Risk Management. This presentation will discuss how Risk Management should be integrated into CAPA systems to help improve CAPA.
Areas Covered in the Session:
An overview of ISO 14971 risk management standard
CAPA system requirements
What are risk-based decisions as stated in FDA's Quality System Regulation Preamble