The aim of the MSc in Regulated New Product Introduction and Technology Transfer is to enable learners to develop their technical and transversal skills to support the transfer of new pharmaceutical and biopharmaceutical products in and out of manufacturing facilities while operating in a GxP regulated environment.

 

Ultimately, graduates will develop fluency in several technical areas including quality, validation and risk management, paperless validation, life science project management in a regulated environment, data analytics and visualization, operations and production suite transfer readiness, Lean Six Sigma skills, research skills, analytical laboratory technology transfer, engineering facilities and utilities. All of these modules will be tuned specifically for the field of new product introduction and technology transfer during their modes of delivery focusing on pharmaceutical, biopharmaceutical, API, and advanced therapies manufacturing.