Making labels comply with MDR
The new European Medical Devices Regulation (MDR) is forcing companies to review their labeling infrastructure as they battle for organisational preparedness
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Search Results for: Mark Cusworth
- Cambridge researchers develop robotic nerve devices for neurological conditions
- International phase 3 clinical trial for new melanoma treatment recruits first patients
- Nova’s Xromi approved in UK and EU for vaso-occlusive complications of SCD
- Study reveals vitamin D-altered mouse gut bacteria provides better cancer immunity
- Cambridge researchers use AI to accelerate drug design for Parkinson’s disease
