Event
Course Description:
This course provides guidance on establishing and implementing a Corrective and Preventive Action (CAPA) program in a laboratory setting. Participants will be introduced to key terms and definitions, followed by a detailed walkthrough of the Corrective Action Program flow, including the requirements for each step. The course also covers commonly used tools for root cause analysis and emphasizes the importance of creating a systematic approach to investigating and resolving identified problems to prevent recurrence.
Pricing varies. Please inquire for more info at https://go.usp.org/Services.
Upon completion of this course, you will be able to
- Understand the purpose and importance of a CAPA program
- Distinguish between key terms and definitions associated with CAPA
- Understand the Corrective Action Program flow and the tools used for root cause analysis
- Implement the CAPA program effectively when a problem is identified
Who should participate:
- National and private QC laboratories (PC, MB, Clinical, etc.)
- Manufacturers