Resource Centre: Latest Updates
Latest regulatory news concerning medical devices and medicines - Feb 2022
There's lots happening in the regulatory world of medical devices. Catch up on the latest news here...
Read moreSoftware as a Medical Device
Software classification has changed with MDR and there is now a rule categorising different types of software when being used as a medical device. Learn more about them here...
Read moreIVDR Regulatory Framework Update
Update to the In Vitro Medical Devices Regulation (IVDR) to ease supply chain challenges
Read moreIVDR Impact on Companion Diagnostics
As the IVDR comes into force in May 2022 understand how the change of regulations impacts Companion Diagnostics
Read moreUnderstanding the latest IVDR Classification Rules
Discover our comprehensive guide to device classification rules for in-vitro diagnostic devices. Download your copy to ensure your products meet the requirements.
Read moreThe 5 types of 3D scanning technology
From scanning an object to reverse engineering it, there are many ways to use 3D scanning to benefit your manufacturing. Discover the 5 different types and advantages for each one in our whitepaper.
Read moreGetting drug-device combinations to market
The key to getting drug-device combinations to market compliantly is in the classification of the product. But what other considerations are applicable?
Read moreRegulatory Update - IVDR Implementation Amendment
EU Commission’s proposed amendment to transition period of the In Vitro Diagnostic Devices Regulation (IVDR) calls for a progressive roll out.
Read moreStudent Placement Blog
In July 2021, Mi3 took on four students from different universities to participate in “A Year in Industry”. Over the course of the year, the students will post multiple blog entries here, to showcase their experiences, highlighting some of the key activities they are involved in.
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