Manufacturers
May 26th 2020: Class I manufacturers, are you ready?
With the fast approaching end of the EU MDR transition period (May 26th, 2020) manufacturers need to ensure their products meet the new requirements by the deadline or risk restricted EU market access. Read more
Manufacturers can now access Global Medical Device Nomenclature for free
The Global Medical Device Nomenclature, the de facto global standard for identifying the world’s medical devices, has been made freely available to all manufacturers for the first time from this week. Read more
MDISS extends ISA guidelines to connected medical devices
The Medical Device Innovation, Safety, and Security Consortium (MDISS) has announced it is developing a set of recommended practices and profiles for securing medical systems. Read more
Investment in high-tech manufacturing essential for the UK, figures show
New productivity statistics from the Office of National Statistics (ONS) show that the manufacturing sector improved its output per hour in the first quarter of this year. Read more
European medical device regulation: What you need to know
Paul Brooks, Regulatory Affairs Professionals Society (RAPS), discusses the impact of European Medical Device Regulation on currently marketed medical devices and offers guidance for manufacturers. Read more
