A QP must certify that each batch of medicinal products complies with its Marketing Authorisation or Product Specification File, GMP plus other requirements depending where manufacture was carried out. The QP must also ensure that they discharge their duties in accordance with the Code
of Practice. This module examines the responsibilities of a QP in depth, including legal and professional duties, how to be an effective QP, certification processes according to Annex 16
and post certification duties. It includes case studies and questions that challenge understanding of the overall role of a QP.
of Practice. This module examines the responsibilities of a QP in depth, including legal and professional duties, how to be an effective QP, certification processes according to Annex 16
and post certification duties. It includes case studies and questions that challenge understanding of the overall role of a QP.
