Curriculum
Course Description:
This course provides a brief overview of the CAPA life cycle, roles and responsibilities, implementation, verification, effectiveness check. Regulatory consequences of incomplete CAPA management (483s, WLs) will also be addressed.
Upon completion of this course, you will be able to:
- Describe challenges associated with CAPA implementation and effectiveness.
- Identify and explain regulatory consequences of incomplete CAPA management (483s, WLs)
- Summarize the roles and responsibilities, effectiveness of implementation of CAPA and verification processes.
Who Should Participate:
- QA Manager
- QA Staff
- QC Manager
- QC Chemist
- Regulatory
USP Approved Instructor
Mr. T Lakshmana Murthy:
Director, Quality assurance at USP-India and chief course designer of the QA course. He has over 21 years of experience in GMP auditing, Quality assurance and regulatory Compliance in the pharmaceutical industry