The European Medicines Agency (EMA) publishes the agendas and outcomes of the monthly plenary meetings of its seven scientific committees.
EMA has been publishing meeting reports summarising the main outcomes of its committees' meetings since they were established. The Agency also publishes the agendas and minutes of all its committees since January 2014.
These documents are available on the respective committees' webpages:
- Committee for Medicinal Products for Human Use (CHMP)
- Pharmacovigilance Risk Assessment Committee (PRAC)
- Committee for Orphan Medicinal Products (COMP)
- Committee for Veterinary Medicinal Products (CVMP)
- Committee on Herbal Medicinal Products (HMPC)
- Committee for Advanced Therapies (CAT)
- Paediatric Committee (PDCO)