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- Registo Investigação e Tratamento de RECLAMAÇÕES : “Muito útil para melhorar os processos já implementados “
- ISO 20417:2026 – Updated Guidance on Medical Device Information – The second edition of ISO 20417:2026 (Medical devices – Information to be supplied by the manufacturer) has just been published.
- COMMISSION DELEGATED REGULATION (EU) …/… amending Regulation (EU) 2017/745 of the European Parliament and of the Council as regards the list of implantable devices and class III devices exempted from the obligation to perform clinical investigations C/2026/1798 final
- Progressing EMA’s PRIority Medicines scheme through new pilot features
- FDA Releases Draft Guidance on Alternatives to Animal Testing in Drug Development
- ‘Pharma package’: Council and Parliament reach a deal on new rules for a fairer and more competitive EU pharmaceutical sector
- EU Pharma Package: Final Texts officially published
- EU COMMISSION Artificial Intelligence Act – detailed arrangements on evaluations and proceedings.