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Most Read

  1. Blood-based PTSD biomarkers in the latest Medical Technology
  2. Deep space diagnostics in the latest Medical Technology
  3. Faulty medical device alerts in UK hit four-year high
  4. Making sustainable medical devices: five top tips
  5. Selling into the NHS: HEE’s top tips for medtech companies

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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. wraps up key headlines from November 2019.

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.

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).

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Medical Technology is the essential reading material for decision-makers in the medical device industry, bringing you the latest news and analysis in an exciting, interactive format.

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