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Key Insights from Early EUDAMED Testing

Key Insights from Early EUDAMED Testing

by Innovit Corporate Affairs | Oct 4, 2022 | Videos

Key Insights from Early EUDAMED Testing & Post Go-Live Feedback Webinar   Lorem ipsum dolor sit amet, consectetur adipiscing elit. Fusce volutpat rhoncus consectetur. Proin sed blandit arcu. Duis scelerisque justo sit amet dui posuere...
Innovit & 1WorldSync: “The Arthrex Journey”

Innovit & 1WorldSync: “The Arthrex Journey”

by Innovit Corporate Affairs | Oct 4, 2022 | Videos

Innovit & 1WorldSync: “The Arthrex Journey” Achieving Data Requirements for UDI   Innovit and 1WorldSync experts discuss the Arthrex Journey” Achieving Data Requirements for UDI & Beyond and the delivery of a PIM Lite...
How to meet the Growing Challenges

How to meet the Growing Challenges

by Innovit Corporate Affairs | Oct 4, 2022 | Videos

Seven years ago when the Federal Drug Administration (FDA) announced its Unique Device Identification (UDI) regulations, there were no off-the-shelf solutions for submitting regulatory data to the Global UDI Database...

Exciting News – Innovit Accepted into Medtech Europe!

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...
We’re Here! Global GS1 Healthcare 2019

We’re Here! Global GS1 Healthcare 2019

by Innovit Corporate Affairs | Mar 26, 2019 | Blog, GS1

Join Innovit on 26 – 29 March in Noordwijk-Amsterdam, The Netherlands The Global GS1 Healthcare Conference, 26-28 March 2019, in Noordwijk-Amsterdam, the Netherlands kicks off TODAY and we’re very excited to get up-to-date on the newest global standards,...
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Recent Posts

  • Regulatory Update: Australia’s UDI Regulation Now in Effect
  • EUDAMED Go-Live Announcement: Streamlined UDI Data Submission using Innovit EUDAMED Connector
  • Updated Timeline: Mandatory Use by Q4 2025 – Current planning for gradual roll out and modules’ functionality view
  • MDR Third Amendment is official: EUDAMED Mandatory Use by January 2026

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