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The Pharmaceutical Quality and Regulation PG Diploma combines specialist good manufacturing practices (GMP) and analysis knowledge with an understanding of local and global legislation, in order to produce quality professionals who can provide long-term solutions to critical manufacturing defects.

About this degree

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 one year. Students can study this course over 5 consecutive years.

Who this course is for

Individuals with a background in pharmacy, pharmaceutical sciences, chemistry, dentistry, medicine, regulation and biology (including all biological sciences) are eligible to apply. Experience in the manufacture, quality and regulation is desirable, but not mandatory.

Employability

The course teaches you to be able to apply a range of academic content and principles needed in pharmaceutical manufacture. You will obtain and demonstrate a range of transferable and problem-solving skills allied to the course content, making graduates highly suited to a career in the pharmaceutical industry in areas associated with manufacturing, quality assurance and regulation.

Duration: Up To 5 Years