Studying at the University of Verona

Study Plan

Your Study Plan includes all the learning activities you will undertake during your time at the University, such as modules, lab activities and practicals, seminars, project work, internships, as well as educational off-site visits, conferences and the final examination, or graduation.

Farmacoepidemiologia 5 Credits

SSD:MED/01

Detail of the Module+
Farmacovigilanza, dispositivo vigilanza e industria 5 Credits

SSD:BIO/14

Detail of the Module+
Farmacovigilanza storia, quadro regolatorio e realta’ italiana 2 Credits

SSD:BIO/14

Detail of the Module+
Health technology assessement 1 Credits

SSD:BIO/14

Detail of the Module+
Il quadro sanitario 1 Credits

SSD:BIO/14

Detail of the Module+
Informazione e comunicazione sui farmaci in fv 3 Credits

SSD:BIO/14

Detail of the Module+
Le reazioni avverse da farmaci 2 Credits

SSD:BIO/14

Detail of the Module+
Metodi in farmacovigilanza 3 Credits

SSD:BIO/14

Detail of the Module+
Nuove frontiere in farmacovigilanza 1 Credits

SSD:BIO/14

Detail of the Module+
Preparazione e presentazione dossier registrativo e richiesta prezzo e rimborsabilita' di un farmaco 2 Credits

SSD:BIO/14

Detail of the Module+
Relazione tra adr e sesso, eta' e specifiche condizioni fisiologiche e patologiche 2 Credits

SSD:BIO/14

Detail of the Module+
Ricerca e sviluppo di un farmaco 3 Credits

SSD:BIO/14

Detail of the Module+
Vaccinovigilanza e fitovigilanza 2 Credits

SSD:BIO/14

Detail of the Module+
E-learning 8 Credits

SSD:BIO/14

Detail of the Module+
Stage 17 Credits

SSD:-

Detail of the Module+
Prova finale 3 Credits

SSD:-

Detail of the Module+

Teaching code

4S005339

Credits

0.33

Language

Italian

Scientific Disciplinary Sector (SSD)

BIO/14 - PHARMACOLOGY

To show the organization of the course that includes this module, follow this link:  Course organization

Learning outcomes

Knowledge of all complex aspects of pharmacovigilance, from scientific to regulatory ones, is one of the general contents of the Master on Pharmacovigilance and Drug Regulations. More general content is the knowledge of the regulatory activities regulating the world of medication, the procedures prior to placing it on the market and the subsequent ones, complex procedures involving the Pharmaceutical Industry and Regulatory Authorities for a continuous activity. Finally, a further general mastery of the Master is knowledge of the vast world of drug information and risk communication from drugs, a task that is mainly carried out in e-learning.

Program

The Master program is available online at the following web page: http://www.medicina.univr.it/fol/?ent=cs&id=502&tcs=M

Reference texts
Author Title Publishing house Year ISBN Notes
Nessuno Per questa attività non sono necessari/disponibili libri di testo 2019

Examination Methods

Attending at least 75% of lessons, stage performance, and the presentation of a final work is mandatory

Bibliography