The Qualified Person must understand the influence of manufacturing pathways and associated physical and physico chemical attributes of both active pharmaceutical ingredients and major excipients on the quality of the finished dosage form.
QP responsibilities also include formally certifying that each Active Pharmaceutical Ingredient (API) is manufactured to GMP, knowledge of the API supply chain and complying with importation requirements as defined in the Falsified Medicines Directive. This course includes both the technical aspects of manufacturing APIs and the requirements of Good Manufacturing Practice.
This is an essential course for all those who expect to be taking the QP Viva, it is also a valuable contribution to Continuing Professional Development for QPs who qualified some years ago. This is also suitable for those who require an understanding of the requirements for manufacturing APIs such as purchasing, manufacturing or regulatory affairs staff.
This 2 day QP module takes place in our purpose built training facilities based on the University of Reading campus in Berkshire
Course cost: £1390 (+VAT)
Learn more and book your place here.
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