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Country-Specific UDI Compliance – Staying Up to Date on Changing Deadlines

by Innovit Corporate Affairs | Apr 14, 2021 | Ashley Howell, Blog, UDI

UDI Timeline: A progression of UDI compliance regulations and deadlines. One thing in healthcare is certain: patient safety and quality of care will continue to drive change in the healthcare market. UDI regulations support this objective and deadlines for...

EUDAMED State of Play – New Playground Available for EUDAMED Device Registration and NBs & Certificates modules

by Innovit Corporate Affairs | Apr 8, 2021 | Ashley Howell, Blog, Eudamed, Industry News, News

What’s New? EUDAMED go-live date is still scheduled for May 2022.  But you may recall that in order to ensure a smooth and effective implementation, the EU Commission provides a “EUDAMED playground.”  It’s currently available for both manual web- based user access,...

Innovit Q&A: M2M Testing – What it means and why it’s important.

by Innovit Corporate Affairs | Apr 1, 2021 | Ashley Howell, Blog, M2M

Medical Device Regulation (MDR) are a set of recent European regulations aimed to enhance patient safety and modernize public health.  Published in May 2017 by the European Commission (EU COM), they are an overhaul and expansion of the MDD (Medical Device Directives)...

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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