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 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 Product Team | Mar 12, 2019 | Blog, UDI
Manufacturers of medical devices and companies that supply them must provide products and services that are both safe and effective. And today’s mounting list of regulations, medical device compliance is important to the success of every medical device manufacturer....
by Innovit Product Team | Feb 26, 2019 | Blog, Eudamed, MDR
With a May 2021 go live date, The European Database for Medical Devices (EUDAMED) will be open to many more groups, including manufacturers, importers and sponsors. Current estimates are that this covers 70,000+ individual organizations and over 300,000 actual users....
by Innovit Corporate Affairs | Nov 5, 2018 | Blog, PIM
Product information management (PIM) systems are expected to grow up to 25.5% by 2023. There is even a growing demand for PIM in the medical field. Specifically, this interest lies in healthcare IT solutions. But what’s the hype all about? Why are those in the...