Second-Level Master Clinical Research and Medical Affairs: Medicines and Medical Devices

Overview

Clinical research is experiencing a new era, both in the field of pharmaceuticals, with the launch of the European portal, and in medical devices (MD), now subject to the new regulation introducing the role of Person Responsible for Regulatory Compliance.

This new professional role must possess the necessary skills in the medical device sector and adequate training to support MD manufacturers in all aspects of the development phases of a new MD in compliance with the new regulation, which will be fully applicable from May 26, 2021. Since this role is now mandatory for all companies, whether internal or external depending on the size of the company, it creates significant opportunities for professional collaboration.

The program is delivered in Italian language; for further information, please contact admissions@unimarconi.com