This webinar will focus on the activities that should be carried out for the establishment and maintenance of a pharmacovigilance system for marketing authorization holders based on quality standards that are detailed in Good Pharmacovigilance Practices. It will also describe the role of the Qualified Person Responsible for Pharmacovigilance in the EU (EU QPPV) as the crucial role in the performance of these activities within the marketing authorization holder’s pharmacovigilance system.
You will get insight into the regulatory framework as well as guidance on the structures and processes of a pharmacovigilance system.