Screenshot of an abstract blue background.

Pharmaceuticals

Role of the Qualified Person

About the Course

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