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:
Who Should Participate:New recruits in he industry with at least 1 year of experience including:
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