Resource Centre: Latest Updates
The must-know clinical evaluation requirements
With the new European Union Medical Device Regulation (MDR 2017/745) replacing the Medical Device Directive (MDD 93/42/EEC) in May 2021, the requirements for clinical evaluation have changed. Read our whitepaper to understand how you’re affected.
Read moreSolvent bonding: the key to bonding medical devices
Looking to secure two medical device components, but not sure how or where to start? Our whitepaper covers all the technicalities of using solvents to bond medical devices.
Read moreHow you can draw on the power of the IoT in healthcare
The Internet of Things (IoT) has made its way to the healthcare sector and is making a positive impact on how healthcare professionals can achieve the best medical outcomes. How can you utilise the IoT right now?
Read moreCE Marking Timeline in the UK Post-Brexit
Still confused about the timelines for CE Marking, EU MDR and the UKCA post Brexit? Our useful infographic should help.
Read moreMi3 joins the Oxford Bioscience Network
Mi3 has become one of the latest organisations to join the Oxford Bioscience Network, or OBN.
Read moreRegulatory Update - Remote Audits for EU MDR/IVDR Certificates
A new notice from the European Commission allows audits to be performed remotely in light of current COVID-19 restrictions. Read more...
Read moreThe benefits of outsourcing your medical device manufacturing
Outsourcing your medical device production to a one-stop-shop contract manufacturer delivers a wide range of benefits for everyone from start-ups to larger organisations. But what are the key benefits?
Read moreRegulatory Update - Human Factors Usability Engineering Guidance
The MHRA has updated their Human Factors and Usability Engineering Guidance....
Read moreMi3 become ‘collaborationeers’ with #UKMfgUnite
UK Manufacturing Unite is a new initiative, created by manufacturers for manufacturers, offering free collaboration between manufacturers.…
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