Master in Drug Regulatory Affairs

The Master in Drug Regulatory Affairs is a two-year postgraduate program for students interested in the pharmaceutical industry, offering a Master degree in Pharmaceutical Sciences.

The curriculum covers pharmaceutical regulations, drug development, and quality assurance, with hands-on training to apply knowledge in real-world scenarios, developing skills in regulatory compliance and quality control.

Graduates can pursue careers as Regulatory Affairs Specialist, Quality Assurance Manager, Compliance Officer, and Drug Safety Associate, finding employment in pharmaceutical companies, regulatory agencies, or healthcare organizations.