by Innovit Corporate Affairs | Sep 4, 2021 | Blog, Eudamed
The European Commission recently sent out an update on the plan for implementation and roll-out of EUDAMED, as it stands today. Changes to the implementation timeline of different modules, and how they will affect the application of each aspect of MDR are outlined...
by Innovit Product Team | Apr 19, 2020 | Blog, GUDID, UDI
The Global Unique Device Identification Database (GUDID) is a database administered by the FDA that will serve as a reference catalog for every medical device with an identifier. Unique Device Identification (UDI) is a system to mark and identify medical devices (via...
by Innovit Corporate Affairs | Jan 6, 2020 | Blog
Happy New Year! As the dust settles from the holiday madness and end-of-year celebrations, we thought we’d take a quick look back and reflect upon our 2019 journey. We’re so fortunate to work with an amazing roster of customers and partners whose relationships are...
by Innovit Corporate Affairs | Sep 24, 2019 | Blog, PIM
There’s a mounting list of regulations aimed towards Unique Device Identification (UDI), intended to improve patient safety, supply chain efficiency and post-market surveillance. The benefits are numerous, but challenges continue for medical device suppliers on their...
by Innovit Corporate Affairs | Sep 5, 2019 | News
San Francisco, CA (September 5, 2019) Innovit, a global software company specializing in Master Data Management (MDM), Product Information Management (PIM), Global Data Synchronization (GDSN) and UDI compliance solutions, has announced their plans for additional...
