Second-Level Master in Pharmacovigilance, Pharmacoepidemiology and Regulatory Affairs

The second-level Master in Pharmacovigilance, Pharmacoepidemiology and Regulatory Affairs is offered by the Department of Experimental Medicine of the University of Campania Luigi Vanvitelli. It is structured in 5 intensive monthly modules, of 60 hours each for 300 hours, with lectures, practical exercises and multiple-choice written assessments. Each module requires at least 18/30 and compulsory attendance is 75%. It includes a final thesis exam. The areas covered are pharmacovigilance, pharmacoepidemiology, regulatory affairs, risk management, drug monitoring and regulations. The pathway is aimed at those who wish to deepen and update their skills, with a structure that links theoretical reflection to concrete applications in the relevant professional context.

The master lasts one academic year, is worth 60 credits and is taught in person in Naples. The language is Italian, with a check of English knowledge. The cost indicated is 2,500 euros.

The aim is to provide specialist skills for pharmaceutical companies, regulatory bodies, CROs and healthcare facilities, with a focus on drug safety and regulations. The career opportunities are Pharmacovigilance Manager, pharmacovigilance officer, drug safety expert, data manager, clinical monitor and pharmaceutical project manager. Upon completion, those who successfully finish the pathway obtain the qualification provided and can use the skills acquired in their own professional field or in further study. Concrete prospects nevertheless depend on each participant's starting profile and experience. Those who work should carefully assess the commitment required, in terms of weekly hours and attendance, to understand whether the programme is compatible with other professional or personal commitments.