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Recentes
European Medicines Agency pre-authorisation procedural advice for users of the centralised procedure
European medicines agencies network strategy to 2028
MDCG 2024-11 – Guidance on qualification of in vitro diagnostic medical devices (October 2024)
Study supporting the monitoring of the availability of medical devices on the EU market
Corrective and preventive action (CAPA) plan assessment: guidance and templates for conformity assessment bodies, notified bodies, designating authorities and joint assessment teams
Iniciativa para melhorar a eficiência na aprovação de novos medicamentos na UE
Consulta pública a decorrer para Projeto de Regulamento de Execução sobre consultas científicas conjuntas de medicamentos
EUDAMED user guide Guidelines on Data Exchange with EUDAMED