Resource Centre: Latest Updates

White Paper

Injection Moulding Series No.1 - Problem Solving

What are the steps involved in identifying potential problems with the injection moulding process, and how do you solve them? All part of the critical steps to ensuring your medical device is a success when launched to market.

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White Paper

Regulatory Series No.1 - Clinical Evaluation Requirements

An outline of the differences between MEDDEV 2.7/1 revision 4 and MDR 2017/745 regarding clinical evaluation..

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White Paper

Design & Development Series No.5 - Solvent Bonding

If you're stuck on how to bond the pieces of a medical device together, solvent bonding just may be the solution you need.

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White Paper

Design & Development Series No.6 - IoT in Healthcare

At Mi3 we often collaborate with third parties to incorporate new technologies into client's products. In this paper, Polymorph discuss how the IoT is disrupting the healthcare sector.

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Guide

CE 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.

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Mi3 News

Mi3 joins the Oxford Bioscience Network

Mi3 has become one of the latest organisations to join the Oxford Bioscience Network, or OBN.

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Mi3 News

Regulatory 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...

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White Paper

Contract Manufacturing Series No.1 - Outsourcing Medical Device Manufacturing

Thinking of outsourcing your Medical Device Manufacturing? Learn how working with a one-stop shop contract manufacturer can present a range of benefits to even the largest of medical device companies...

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Mi3 News

Regulatory Update - Human Factors Usability Engineering Guidance

The MHRA has updated their Human Factors and Usability Engineering Guidance....

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