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Let us help you on the path to UDI Compliance for FDA with Innovit’s GUDID Reference Center

Let us help you on the path to UDI Compliance for FDA with Innovit’s GUDID Reference Center

by Innovit Corporate Affairs | Mar 24, 2022 | Blog, Michelle Laurion, UDI

Are you preparing for the FDA’s enforcement of UDI labeling and GUDID (Global Unique Device Identification Database) data submission requirements for Class I and unclassified devices, coming up in September 2022?  Your company should start to aggregate, validate and...

We’re Excited To Be Back In Person! Announcing Innovit’s 2022 Event Calendar

by Innovit Corporate Affairs | Mar 3, 2022 | Blog, Michelle Laurion

As we look ahead with optimism to traveling again in the coming year, with some expected bumps along the way, we’re thrilled to share Innovit’s return to in-person events in 2022!  No doubt we’ve all gained some new appreciation for ‘real’ in-person events – so we...

Recent Posts

  • 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
  • TGA’s Australian UDI Database: Deadline Update

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