Class I manufacturers who snooze will lose trade access to EU markets
Class I medical device manufacturers must act now to meet new regulations
Maetrics appoints new director of global clinical practice
Tackling clinical evaluation head on
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
10 top tips to conform with the new Medical Device Regulation
From Scan4Safety to UDI: Unique identifiers for the UK
Manufacturers – it's time to prepare for Unique Device Identification (UDI)
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
