by Innovit Corporate Affairs | Jun 26, 2019 | Blog, MDM
Healthcare providers are increasingly putting emphasis on a patient-centric approach to care delivery. From ensuring patient safety to providing quality care at an affordable cost, care providers have embraced healthcare information technologies as a cornerstone to...
by Innovit Corporate Affairs | Jun 3, 2019 | Blog, GUDID
In 2014, the seven-day grace period for Global Unique Device Identification Database (GUDID) submission corrections was extended to 30 days. Over time, healthcare providers provided feedback stating that 30 days is too long to wait for access to “key...
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...
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....