by Innovit Corporate Affairs | Aug 14, 2019 | Blog, GDSN
The goal of UDI is to help improve patient safety by enabling better traceability of medical devices consumed. For the ‘labeler’, UDI will help improve internal processes, bolster master data quality, and provide more accurate reporting and visibility related to...
by Innovit Corporate Affairs | Jul 18, 2019 | Blog, MDR
Keeping up with the evolving medical device regulation and compliance landscape can be challenging, particularly when technical specifications from the EU Commission are repeatedly delayed. As a global software solution vendor for Life Sciences and Healthcare...
by Innovit Corporate Affairs | Jul 15, 2019 | Blog, Eudamed
Keeping up with the evolving medical device regulation and compliance landscape can be challenging, particularly when technical specifications from the EU Commission are repeatedly delayed. As members of MedTech Europe and Healthcare Transformation Group, we’re doing...
by Innovit Corporate Affairs | May 28, 2019 | Blog, Eudamed
As it prepares to meet new regulatory requirements in Europe, the medical device community is following developments regarding the European Database for Medical Devices (Eudamed). Most recently, the European Commission (EC) released three documents for Medical Device...
by Innovit Corporate Affairs | Apr 15, 2019 | Blog
Innovit, a global MDM and PIM solutions, has been accepted into Medtech Europe and the Medtech Europe Corporate Council as a corporate associate member. The Council is an invitation-only community representing In-Vitro Diagnostics and Medical Devices manufacturers...