Pharmaceutical Quality and Regulation PG Dip

Students will learn how to manufacture and test various pharmaceutical dosage forms, production planning and inventory control, method validation, quality risk management, and regulatory aspects such as the development and assessment of clinical trial dossiers. The programme will expose you to a range of investigational strategies for dealing with critical incidents during the manufacture of pharmaceuticals.

Students can study this course on a full-time or on a flexible basis. If studying full time the course duration is 1 year. Students can study this course over 5 consecutive years.