Guidance
Clinical investigations for medical devices
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
News & Trends
Procurar
Recentes
- EMA Updates Guidance on National Pharmacovigilance Contact Person Requirements
- ICH E20 draft guideline on adaptive designs in confirmatory clinical trials
- Critical shortages of medicines. European Court of Auditors’ Special Report
- EDQM publishes new guidelines on the classification of active pharmaceutical substances as regards their supply
- Clinical Evidence Requirements under the EU In Vitro Diagnostics Regulation (IVDR). MEDTECH E-BOOK
- A Formiventos está novamente no ranking das Top 5% melhores PME de Portugal
- Manual on borderline and classification for medical devices under Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnostic medical devices Version 4 – September 2025
- ICH adopts M14 guideline on observational studies