by Innovit Corporate Affairs | Oct 16, 2019 | News
We are so proud to announce that after the initial round of EUDAMED Playground M2M Data Exchange testing, Innovit was the only solution provider able to successfully complete all the test cases for Device/UDI Registration. Those test results were published by the EU...
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 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 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 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...
