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Complying with UDI & MDR: Facts, Figures and Action Items

Complying with UDI & MDR: Facts, Figures and Action Items

by Innovit Product Team | Mar 12, 2019 | Blog, UDI

Manufacturers of medical devices and companies that supply them must provide products and services that are both safe and effective.  And today’s mounting list of regulations, medical device compliance is important to the success of every medical device manufacturer....
Leveraging Your Wealth of Healthcare Data for Better Patient Care

Leveraging Your Wealth of Healthcare Data for Better Patient Care

by Innovit Corporate Affairs | Feb 7, 2019 | Blog, MDR

Innovit at GS1 UK Healthcare Conference, London   Managing the wealth of available healthcare data allows health systems to create holistic views of patients, personalize treatments, improve communication and enhance health outcomes. Additionally, data continues...
The Most Common Mistakes in NPI Process and How to Avoid

The Most Common Mistakes in NPI Process and How to Avoid

by Innovit Corporate Affairs | Aug 27, 2018 | Blog, NPI

New Product Introduction (NPI) is a complicated and highly collaborative process. And that means there’s a lot of room for error. These errors are very expensive and can slow down the whole NPI process. Worst of all, they may go undetected until the launch. Can...
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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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