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.
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.
