Artigos recentes
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- Questions and Answers on repackaging & relabelling activities under Article 16 of Regulation (EU) 2017/745 and Regulation (EU) 2017/746
- Regulation (EU) 2017/745 – application of MDR requirements to ‘legacy devices’ and to devices placed on the market prior to 26 May 2021 in accordance with Directives 90/385/EEC or 93/42/EEC
- PROMOTIONAL REVIEW 2021: “Excelente formação “
- 4ª Edição da formação sobre GMP para Canábis : Vagas esgotadas
- ICH announces sign-off on good clinical practices guideline. E8(R1):GENERAL CONSIDERATIONS FOR CLINICAL STUDIES
- MDCG 2021-24 Guidance on classification of medical devices. October 2021
- INFARMED : AUE de benefício clínico bem reconhecido: alteração do procedimento