Resource Centre: Latest Updates
Mi3 joins Reshoring UK Initiative
Mi3 has become the latest company to join the Reshoring UK initiative, a unique collaboration of leading industrial engineering associations to assist…
Read moreYour free guide to current MDR Classification Rules
The classification of medical devices has changed with the implementation of the EU MDR. See how you’re affected in our handy infographic and complete guide.
Read moreUtilising the IoT in Medical Devices
The Internet of Things (IoT) is shaking up the healthcare industry. Learn more about our new white paper on how utilising IoT technology in medical devices can positively impact on overall healthcare processes and patient experience...
Read moreThe Benefits of MDSAP Acreditation
While there are approval routes that don’t require your devices to be developed and manufactured under an ISO 13485 quality management system,…
Read moreThe definitive guide to IFU for Medical Devices
We’ve collaborated with INSTRKTIV to share the definitive guide to IFU for medical devices and in-vitro diagnostic products. Discover all the requirements for both the US and EU markets.
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