The Council of the European Union has published a second set of corrections as part of a corrigendum for the EU’s Medical Devices Regulation (MDR), this time giving manufacturers of certain Class I devices an additional four years to comply.
News & Trends
Procurar
Recentes
- HERBAL FOOD SUPPLEMENTS Guide for healthcare professionals
- FDA eCopy Program for Medical Device Submissions
- Dezember 20025: key takeaways on the critical medicines act, the pharma package and more
- BOAS PRÁTICAS DE DISTRIBUIÇÃO DE MEDICAMENTOS : “Informativo e esclarecedor “
- Study supporting the monitoring of the availability of medical devices on the EU market
- EAHP 2025 Shortages Survey Report
- EUDAMED MILESTONE : Implementation Timelines Confirmed
- Amending Regulations (EU) 2024/1689 and (EU) 2018/1139 as regards the simplification of the implementation of harmonised rules on artificial intelligence (Digital Omnibus on AI)