Master of Science (M.Sc.) in Regulatory Affairs typically spans 1-2 years and is designed for professionals aiming to navigate the complex regulatory landscape of industries such as pharmaceuticals, biotechnology, and medical devices. The program covers essential topics, including regulatory compliance, quality assurance, and the drug development process. Students learn about the regulations governing product approval, post-market surveillance, and the legal aspects of product safety. The curriculum often includes case studies and practical experiences to equip graduates with the skills needed to work effectively in regulatory agencies or within corporate regulatory affairs departments, ensuring products meet legal and safety standards.
