Role of the Qualified Person

The role of the Qualified Person (QP) is defined in European Union legislation. This course explains the release of medicinal products to the market, the release of clinical trial materials, and pharmacovigilance. Topics in this course include: Regulation, Qualifications/Codes of Practice, Batch Certification, Different Supply Situations, Clinical Trials, and Pharmacovigilance. After completing this course, learners will be able to identify the role and responsibilities of both types of QP defined in EU legislation.

After this course learners will be able to identify the role and responsibilities of both types of qp. recognize how these fit within eu legislation.