Class I manufacturers who snooze will lose trade access to EU markets
Class I medical device manufacturers must act now to meet new regulations
The European Union Medical Device Regulation (MDR): One year on
Comment: The new In Vitro Diagnostic Medical Device Regulation – challenging times ahead
The Medical Device Regulation (MDR) – why it pays to act quickly
The Medical Device Regulation – why it pays to act quickly
An in-depth guide to the Medical Device Single Audit Programme
10 top tips to conform with the new Medical Device Regulation
From Scan4Safety to UDI: Unique identifiers for the UK
Calling all MedTech manufacturers – it’s time to ramp up post market surveillance
Clinical Evaluation Reports that always pass the test
Medical Device Regulations Training Course
Lighting the way - lighting for operating theatres
Synergy Health launches advanced surgical instrument pre-clean gel
