Event
Course Description:
This two hour 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:New recruits in he industry with at least 1 year of experience including:
- Quality Assurance
- Quality Control
- Analytical
- Regulatory Affairs
- Engineering
- Manufacturing personnel working in Pharma and allied industries.