Course Description

The quality of a medicine depends in no small part on the quality of its ingredients, and in particular the active. Thus, the Qualified Person and other key professionals in dosage form manufacture must have a thorough understanding of how the manufacture and control of the active and its supply chain may influence the fitness for use of the finished product. This is recognised by the regulators, especially in Europe where the adoption of Directive 2004/27/EC has put the responsibility for assuring the quality of the active firmly on the shoulders of the dosage form manufacturer, with certain expectations specifically for the QP. This course is designed to provide you with the knowledge and understanding to fulfil your responsibilities with competence and confidence.

Learn More