MSc in Development and Regulation of Medical Technologies

Development and Regulation of Medical Technologies
(Development and Implementation of Pharmaceuticals)

Year 1:

Semester A:

Biostatistics (0103-0012), mandatory faculty course.

Epidemiology (0158-1011), mandatory faculty course.

Drug Development (0103-5075), Dr. Oren Becker.

Semester B:

Medical Device Development (0103-5086), Dr. Nadav Sheffer.

The Israeli Regulatory System (0103-5077), Dr. Osnat Luxenburg and the Directorate team.

Regulation and Law (0103-5078), Adv. Liad Shoham.

Principles of Intellectual Property (0103-5079), Dr. Gal Ehrlich.

Summer Courses:

010350810 – Introduction to US Commercialization of Life Sciences Companies
Eran Steinberg

010350820 – Vaccines Clinical Development
Dr. Frederick Wittke

010350830 – Biomedical Software Regulation
Dr. Thomas Colonna and Jonathan Helfgott

Year 2:

Semester A:

Artificial Intelligence in Drug Development (0103-5092), Dr. Yair Benita.

Fundamentals of Clinical Research (0103-5084), Prof. Ravit Geva.

Global Regulatory Systems and Processes (0103-5085), Dr. Michal Roll.

Semester B:

Biologics, Advanced Therapies and Bio convergence (0103-5074),
Dr. Michal Rol and Dr. Anat Gloverzon-Levin.

Development, Production and Quality Control of Biologicals (0103-5087),
Ms. Rivka Zaibel.

Pharmacovigilance and Clinical Safety (0103-5089),
Dr. Hedva Volvovitch.

Regulatory Science Seminar (0103-5093),
Dr. Michal Roll.

Regulatory Writing (0103-5094),
Dr. Shiri Diskin – Pharmaceuticals,
Shoshana Friedman – Medical Devices.