Blood-based PTSD biomarkers in the latest Medical Technology
In this issue: blood-based biomarkers for PTSD, transvaginal mesh, reversing Alzheimer’s memory loss,...
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Deep space diagnostics in the latest Medical Technology
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Faulty medical device alerts in UK hit four-year high
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Making sustainable medical devices: five top tips
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Selling into the NHS: HEE’s top tips for medtech companies
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The future of bioprinting: A new frontier in regenerative healthcare
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To the bone: improving scaffolds using 3D printing
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DIAMOND Showcases Expanded Beam (XB) Lensed Ferrule Connector Series
DIAMOND SA, a leader in high precision fiber optic interconnect solutions, presents the Expanded Beam (XB) lensed ferrule series.
November’s top news stories
Researchers at the University of Toronto and Arizona State University have developed a direct gene-circuit-to-electrode interface for the conversion of biological information into an electronic signal, and Zebra Medical Vision has secured 510(k) clearance from the US FDA for its AI-powered HealthCXR device. Medicaldevice-network.com wraps up key headlines from November 2019.
Blood-based PTSD biomarkers in the latest Medical Technology
In this issue: blood-based biomarkers for PTSD, transvaginal mesh, reversing Alzheimer’s memory loss, redesigning medical devices, and much more.
Deep space diagnostics in the latest Medical Technology
In this issue: Deep space diagnostics, dirty duodenoscopes, smartphone-based sperm testing, at-home asthma management, and much more.
Sandvik – Walk the Talk
Sandvik achieved a top score in a sustainability report presented yesterday by Misum, Stockholm School of Economics. We not only talk about sustainability; we also get things done.
Abbott to build medical device manufacturing facility in Indiana
US-based medical devices maker Abbott Laboratories has announced plans to build a manufacturing facility in Indiana, a move that is expected to create over 450 jobs.
Design and Branding of the New Phaco System
It proves extremely useful to already deal with brand development at an early stage and professionally.
General Safety and Performance Requirements
The heart of the European Union (EU) regulation of in vitro diagnostic medical devices (IVDs) lies in allowing market access to IVDs that offer clinical benefit, and are safe to the patient, the user of the IVD and others (such as service technicians).
Automation Solutions for Testing
Mikron's automation solutions are developed to run around the clock and provide you with the best service.
India’s Health Ministry to scrutinise all medical devices under CDSCO
India’s Union Health Ministry has announced that medical devices intended for human and animal use will go through the scrutiny of the Central Drugs and Standard Control Organisation (CDSCO).
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