by Lionel Tussau | May 25, 2021 | atrify News, Featured Post, Healthcare News, Industry, News
On 26th May 2021, the EU Medical Devices Regulation (MDR) finally came into full application, superseding the former medical device directives from the 1990's. EUDAMED has been live since December 2020 (Actor Registration module) and its 2 next modules (UDI and...
by Lionel Tussau | Apr 13, 2021 | atrify News, EUDAMED News, Healthcare News, News
There are currently a number of regulatory changes in the healthcare industry that companies need to follow closely - and we're here to help. Firstly, changes to the EUDAMED deadlines for the UDI and device registration module will make it easier for the industry to...
by Lionel Tussau | Apr 7, 2021 | atrify News, Healthcare News, Industry, News, News-de, Partner
We are pleased to announce the new partnership between atrify and @GP. The French market will therefore benefit from the best of both solutions and expertise - atrify having built a successful connector to EUDAMED and other regulatory UDI databases in the world...
by Lionel Tussau | Mar 3, 2021 | atrify News, EUDAMED Blogs, EUDAMED News, Healthcare News, News
EUDAMED is getting closer every day and testing is about to restart for the last UDI registration playground before going live in a couple of months. Time is getting short for companies to get their processes and UDI data in order. How to be compliant with the MDR...
by Lionel Tussau | Jan 5, 2021 | atrify News, EUDAMED Blogs, EUDAMED News, Healthcare News, News
As a leading provider of product content solutions, we are pleased to announce that healthcare manufacturers are now able to send their data to Resah via the Global Data Synchronization Network (GDSN) for consolidated and reliable...