Whether using a computer to draft, engineer or manufacture (CAD/CAE/CAM), analyze and simulate, or simply managing the endless documentation and details of a product’s lifecycle, specialized ...

Legacy medical devices face growing scrutiny as regulators push for stronger cybersecurity, transparency and risk management.

Many medical device companies develop software using a traditional waterfall methodology in which each step is taken in sequence: requirements, design, implementation, verification, and validation ...

In a member webinar hosted by techUK, experts from the Medicines and Healthcare products Regulatory Agency (MHRA) provided a comprehensive introduction to the UK’s regulatory framework for software as ...

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There has been a surge in academic and business interest in software as a medical device (SaMD). It enables medical professionals to streamline existing medical practices and make innovative medical ...

Medical device cyber challenges are among the most complex for manufacturers and healthcare delivery organizations for a variety of reasons, but there are some ...

Sophisticated clinical software systems employed in specific health care services have graduated from being interfaces, operating systems, and subordinate tools that support physical medical devices ...

Dublin, Feb. 25, 2026 (GLOBE NEWSWIRE) -- The "Global Market Access for Medical Device Software Training Course (June 8th - June 9th, 2026)" training has been added to ResearchAndMarkets.com's ...

The latest update to the Federal Drug Administration (FDA) for medical device cybersecurity mandates the development of a software bill of materials (SBOM). This provision can be a significant ...