Pharmaceutical regulatory affairs is the science of ensuring that drugs and other therapeutic products are safe and effective.

The primary objective of this Masters is to enable learners to expand their job responsibilities and opportunities in new areas after completing the programme.

The Master of Science in Regulatory Affairs program will prepare you to manage global processes for organizations involved in developing and seeking marketing ...

The mission of the Master of Science program in Drug Regulatory Affairs is to prepare students to become lifelong learners and leaders in a variety of settings.

The curriculum offers courses from pharmaceutical science and regulatory affairs (RA) and quality assurance (QA), bridging the gaps in knowledge that often ...

A unique opportunity to study aspects of regulatory affairs at an advanced level. This part-time course is designed for busy regulatory professionals.

The MSc in Drug Regulatory Affairs is an international programme focusing on the regulation of medicinal, biological and biotechnological products, as well as ...

This course will develop knowledge of the design, development, analysis and production of medicines, the drug industry and regulatory affairs.

This program, which combines online and in-person learning opportunities, takes approximately two years to complete. Curriculum · Admission Requirements · Tuition

The Master's Programme in Pharmaceutical Sciences provides knowledge of drug development and focuses on the qualitative process of drug approval.