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National competent authorities are invited to attend this session for a progress report on UPD Data Quality Framework

Event Veterinary Medicines

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.

Event Human Pharmacovigilance

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

Event Human Veterinary

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.

Event Human Paediatrics