by Innovit Corporate Affairs | Oct 16, 2019 | Blog, Eudamed
EUDAMED deadlines remain unchanged – the go-live date is still March 26, 2020 with the Date of Application for device registration/submission standing at May 26, 2020. Yet, we’re nearing the end of 2019 with most med device companies still struggling to fully...
by Innovit Corporate Affairs | Sep 19, 2019 | Blog, UDI
If you’re a medical device manufacturer or supplier submitting data to the FDA’s GUDID system, then your life may be getting a bit more complicated if you’re also using PTC’s UDI solution to comply with this FDA regulation. Recent announcements suggest that PTC is...
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 | Jan 30, 2019 | Blog, Eudamed, MDR
We’re attending the GS1 Global Healthcare Conference! Master data is at the center of important initiatives within healthcare including patient safety, post-market surveillance, supply chain optimization and regulatory compliance. While manufacturers have...