Course Description:
This course introduces the revised WHO Good Practices for Pharmaceutical Quality Control Laboratories (GPPQCL), providing participants with a clear understanding of the updated guidelines and their practical implications. The session begins with an overview of the purpose, scope, and benefits of adhering to the GPPQCL standard, followed by a detailed explanation of the structure of the revised requirements and the major changes from the previous version.
Participants will also explore strategies for effective good laboratory practices implementation as per WHO GPPQCL guidelines and review the process for preparing and attaining WHO Prequalification (PQ) status.
Pricing varies. Please inquire for more info at https://go.usp.org/Services.
Upon completion of this course, you will be able to
- Explain the purpose, scope, and benefits of complying with the revised GPPQCL standard.
- Recognize the structure of the requirements and highlight major changes from the previous version.
- Identify strategies for implementing the revised guidelines.
- Recall the process for preparing and achieving WHO PQ status.
Who should participate:
- National regulatory authorities
- National control laboratories
- Private QC laboratories
- QC lab in manufacturer