CAPA Management Foundation
Course Description:
CAPAs, or Corrective and Preventative Actions, are an important part of GMP compliance. By their very nature, CAPAs address issues that have already caused problems, and so their primary focus is on corrective action. However, CAPAs can also be used to prevent future problems from occurring. In order to be effective, CAPAs must be based on a thorough understanding of the root cause of the problem. Once the root cause has been identified, CAPA teams can develop SMART actions which are specific, measurable, achievable, relevant, and time-bound. By following these best practices, CAPAs can help organizations to avoid future compliance issues and ensure a high level of quality in their products. This training module will provide an overview of CAPAs in GMP environments and discuss best practices for their development and implementation.
Learning Outcome:
- Define what is a CAPA
- Explain why it is important to raise CAPAs
- Explain how to raise them
- Explain the process of recording issues in the CAPA management system
- Identify the different roles involved in the CAPA process and system
- Define what is a CAPA
- Explain why it is important to raise CAPAs
- Explain how to raise them
- Explain the process of recording issues in the CAPA management system
- Identify the different roles involved in the CAPA process and system
Course Features
| Modules | : | 1 |
| Duration | : | 45 Minute(s) |
| Language | : | English |
| Assessment | : | Self |
| Skill Level | : | Entry |
Course Content(s)
CAPA - Introduction (CPCP0101)
This module will take you through what CAPAs are, why they are raised and monitored and how this is achieved in a GMP environment. It covers the basics of who is involved in raising, recording and reviewing them and why it is important to have a systematic process of dealing with them.