April News & Events

We've now entered Spring season and like all of you, are eagerly watching for news that the EC Proposed Amendment passes. On January 23, 2024, the European Commission proposed a legislative amendment to address two major issues in the EU Medical Device Regulation (MDR) and the In Vitro Diagnostics Regulation (IVDR). See the updates and key changes in our recent blogs.?

You are invited! Reed Tech is hosting several upcoming live webinars that will dive into specific scenarios for UDI with invited panelists from industry. If you can't make the date, no worries, go ahead and register for the recording link and slides. We are looking forward to some insightful discussions with industry experts from AKRA TEAM, Greenlight Guru and Cisema.?Click on the graphics to register below and learn more about our panelists.

Recent Blogs

EC Proposal Updates on IVDR Transition & EUDAMED Rollout (short videos)

See some quick insights from our experts on the EC Proposal concerning the IVDR transition and proposed MDR/IVDR amendment, possibly affecting the EUDAMED rollout. These are short segments created from our latest presentation, prepared exclusively for UDI customers.?

Learn more

Expert Insights on the EU Proposed Legislation EUDAMED Rollout

Our in-house expert, Gary Saner, explains proposed changes to MDR and IVDR and how they could impact medical device manufacturers.

Learn more

Reed Tech Submits First M2M Submission to the AusUDID Preproduction System

Ensure your team is covered for UDI in Australia. As part of the working pilot group, Reed Tech became the first company to submit a device record (machine-to-machine) to the AusUDID Pre-Production system successfully.

Learn more

Contact Us

If you have questions around planning and strategy or just need help with regulatory matters in preparing for UDI submissions to global health authorities, please feel free to contact us via email at [email protected].?