
07-14
2025
EU | Master UDI-DI Implementation Timelines for Optical Devices

07-14
2025
EU | On expert panels' admin and adding a medical devices panel

07-14
2025
EU | Amending Regulation on eIFU of Medical Devices

07-14
2025
EU | Eases Device Instructions for Healthcare Digitalisation

06-30
2025
EU | Interplay between the MDR & IVDR and the AIA

06-30
2025
EU | Regulation Q&A on IVD Medical Devices Performance Studies

06-30
2025
EU | Guidance on the safe MDSW apps on online platforms

06-30
2025
EU | Guidance on Qualification and Classification of Software

06-30
2025
FDA | Transfer of Premarket Notification (510(k)) Clearance Q&A

06-30
2025
EU | Master UDI-DI for high individualised devices
