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Recentes
- 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
- Electronic Systems, Electronic Records, and Electronic Signatures in Clinical Investigations: Questions and Answers
- Reflection paper on the use of Artificial Intelligence (AI) in the medicinal product lifecycle
- Guidance for best practices for clinical trials