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NAMDET has expanded to Facebook.
To access just go to Facebook and type in NAMDET, there are many photographs uploaded already.

This is an open group

MDET Journal, July 2025

Please see the link to the latest edition of MDET the Medical Device Educators and Trainers journal. NAMDET is sharing good news, looking at innovations and also new articles around device disinfecting and cleaning chemicals, safety initiatives as well as launching the latest NAMDET e-learning course for ‘beds, bed rails and trolleys’ to help with …

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Help on MSc Medical Device Training Research

A NAMDET colleague is looking for help in completing their MSc research project around medical device training and wonders if anyone can help? Tisha is a final-year Biomedical Systems Engineering student at the University of Warwick, currently working on a dissertation alongside MTS Health. Their research focuses on optimising medical device training through policy enhancements …

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FDA release draft report into pulse oximeters

The Food and Drug Administration have released much-anticipated testing recommendations for pulse oximeters. The draft guidance follows years of discussion about concerns that the devices can be less accurate for people with darker skin pigmentation than people with lighter pigmentation.

Review of digital clinical safety standards: DCB0129 and DCB0160

NHS England has commenced a review of digital clinical safety standards DCB0129 and DCB0160 to ensure they remain up-to-date, practical and aligned with the latest advancements in healthcare technology and clinical practice. They are actively seeking input from a range of stakeholders, including NHS professionals, IT manufacturers and those involved in digital risk assessment. This will support them to …

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MHRA Consultation; Medical Devices Regulations: Routes to market and in vitro diagnostic devices. Closing date 5th January 2025

NAMDET members are asked to look at the latest MHRA consultation and make recommendations, suggestions etc. Closing date is January 5th 2024. Please feel free to share with colleagues working in medical device design and development too. The MHRA is inviting members of the public – including patients, medical device researchers, developers, manufacturers and suppliers, …

MHRA Consultation; Medical Devices Regulations: Routes to market and in vitro diagnostic devices. Closing date 5th January 2025 Read More »

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