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.
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.
The Master program is available online at the following web page: http://www.medicina.univr.it/fol/?ent=cs&id=502&tcs=M
Per questa attività non sono necessari/disponibili libri di testo
Attending at least 75% of lessons, stage performance, and the presentation of a final work is mandatory