A Qualified Person (QP) must certify that each batch of medicinal product complies with its Marketing Authorisation or Product Specification File, GMP and certain other requirements.
Their conduct overall must comply with the Code of Practice for QPs.
This module examines the responsibilities of a QP in depth, including case studies and questions that challenge the attendees' knowledge of the Code and of the Guide to Good Manufacturing Practice.
Their conduct overall must comply with the Code of Practice for QPs.
This module examines the responsibilities of a QP in depth, including case studies and questions that challenge the attendees' knowledge of the Code and of the Guide to Good Manufacturing Practice.
