MSc in Development and Regulation of Medical Technologies

The curriculum blends rigorous academic training with practical insights from industry experts, offering a comprehensive understanding of the entire lifecycle of medical products. Courses cover diverse topics such as drug development, medical device regulations, software as medical devices, development and production of vaccines, biologics and advanced therapies (e.g. bioconvergence products), pharmacovigilance, legal fundamentals of regulations, intellectual property, AI in drug development, clinical trials, Israeli and global regulatory systems. With a focus on practical application, students engage in specialized seminars, regulatory writing workshops, and internship opportunities tailored to their career aspirations.