Program Overview

Master in Clinical Research: Methodology, Pharmacovigilance, Legal and Regulatory Aspects

Program Overview

The Master in Clinical Research: methodology, pharmacovigilance, legal and regulatory aspects is a comprehensive program designed to provide foundational and specialized knowledge in all aspects of clinical trial organization and management related to pharmaceuticals, medical devices, food, and cosmetics. This program is tailored for individuals interested in developing a specific professional expertise in the field of clinical trial design, management, and monitoring.

Program Details

• ID: 27695
• Course Type: Master
• Academic Year: 2022/2023
• Degree Level: M2
• Length: Annual
• Tuition Fee: 4000
• CFU: 60

Educational Goals

The Master program aims to achieve an educational pathway focused on providing basic and specialized notions related to all aspects of clinical trial organization and management. It is directed towards subjects interested in developing a specific professional expertise in the field of clinical trial design, management, and monitoring.

Program Structure

The program's structure includes:

• Ordinamento: Objectives, learning outcomes, tuition fees, and other educational information.
• Piano Formativo: Admission requirements, selection process, faculty, educational activities plan, and delivery methods.
• Come Iscriversi: Instructions for submitting an application for admission and payment deadlines.

Department and Faculty

• Department: Medicina traslazionale e di precisione
• Faculty: Facoltà di Medicina e Odontoiatria
• Location: Roma, Italia
• Director: Marcello Arca

Program Duration and Admission

• The program is annual, with a deadline for application submission by 16 January 2023.