Events


The Committee for Medicinal Products for Veterinary Use (CVMP) is the committee that is responsible for preparing the Agency's opinions on all questions concerning veterinary medicines.

Event Veterinary Medicines

This is a webinar on SPOR and xEVMPD during which EMA’s SPOR team will cover all aspects of regulatory data management and the way SPOR and xEVMPD work.

Event Human Medicines Data on medicines

EudraVigilance is the EU's system for managing and analysing information on adverse reactions to medicines which have been authorised or are being studied in clinical trials in the European Economic Area (EEA) and supports the reporting and analysis of suspected adverse reactions originating from clinical trials and the post-authorisation phase of...

Event Human Clinical trials

This meeting between European Medicines Agency (EMA) and COCIR is organised in the context of the EMA annual bilateral meetings with industry stakeholder organisations.

Event Human Advanced therapies