CAPA is the merging of change control, continuous improvement, and complaint management.
That means that CAPA is the heart of the quality management system.
CAPA not only indicates the organization's ability to respond to problems but also to anticipate and prevent subsequent problems from arising.
This event highlights:
- The various regulations governing CAPAs
- How CAPAs are successfully initiated and managed
- How CAPA is an integral part of the quality system
- How an effective failure investigation and root cause analysis is accomplished.
During this webinar, emphasis is placed on the application and practical aspects of the process to include its critical steps, CAPA timing, participants to the process, roles and functions, and the pitfalls associated with CAPA investigations.
At the completion of this webinar, you will be able to:
- Explain the purpose and function of CAPA
- Identify and explain the relevant CAPA regulations
- Define exception/deviation reporting and explain the process of executing the reporting process
- Explain and trace the CAPA flow from problem identification to resolution
- Explain the challenges and pitfalls of the CAPA process and how they are overcome
- Explain CAPA's role in risk mitigation
- Explain how root cause analysis is executed
- Charles H. Paul, President of C. H. Paul Consulting, Inc
- CAPA Defined
- CAPA Relevant Regulations
- Exception/Deviation Reporting
- CAPA Process Flow
- CAPA Process Steps Explained
- Challenges and Pitfalls of CAPA's
- CAPA and Risk Mitigation