EU MDR Update: How To Get a New Medical Device Certified? [Flow Charts]

If you are developing a new medical device for sale in the EU, the EU MDR update affects you as you must now get it certified to the EU MDR regulation.  But what is the path to get it certified? … Continue reading →

Since May 2021, the New EU MDR Medical Device Regulation 2017/745 is in place. One of its objectives has been improving the safety of users and patients. And one way to achieve that objective is ensuring that all the parties involved … Continue reading →

If you make, import, or distribute products that end up on the European Union market, and if your products may be categorised as medical, you need to be very clear about that. As we discussed recently, the companies involved in … Continue reading →

Our CEO Renaud is joined again by Clive Greenwood, a China-based product compliance expert, to discuss the new EU MDR. We all heard about the Wild West of PPE imports in the early days of the pandemic where worrying amounts of substandard … Continue reading →