Tag: Medical Devices Regulation
UK government confirms indefinite recognition of CE-marked medical devices
The UK government has confirmed that it will continue to accept CE-marked medical devices on a long-term basis, meaning devices and in vitro diagnostic...
Update on regulatory landscape points to benefits of global collaboration
At the 2019 Vascular Interventional Advances (VIVA) conference in Las Vegas, USA (4–7 November), Misti Malone (US Food and Drug Administration Office for...
Europe braces for harder times in medical device innovation while US...
Countries in the European Union have long been the first to receive new innovations in medical technology, as the EU’s Medical Device Directive (MDD)...
