Events


The Pharmacovigilance Risk Assessment Committee (PRAC) is the committee that is responsible for assessing all aspects of the risk management of medicines for human use.

EventHumanPharmacovigilance

This is the fourth system demo organised by EMA as part of its agile transformation in 2023.

EventHumanVeterinary

The Paediatric Committee (PDCO) is the committee that is responsible for assessing the content of paediatric investigation plans, which describe how a medicine should be studied in children, as well as waivers and deferrals.

EventHumanPaediatrics
EventHumanMedicinesResearch and development

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

EventHumanMedicines