Medical device companies, especially those with real-time embedded-system products, are often burdened with lengthy verification cycles. Even small development efforts can result in months of ...

Software testing, verification and validation form the backbone of modern software quality assurance. These interrelated activities ensure that a software system accurately implements its intended ...

A well-repeated truism throughout the semiconductor industry is that chip design verification is complex and often takes up the largest portion of a design project’s schedule –– sometimes as much as ...

While the disciplines of functional verification and test serve different purposes, their histories were once closely intertwined. Recent safety and security monitoring requirements coupled with ...

Wearable, mobile, implantable, and home health devices as well as electronic components, circuit boards, and subassemblies incorporated into medical equipment used in clinical settings all present ...

This article is a condensed version of an article that appeared in the November/December 2022 issue of Chip Scale Review. Adapted with permission. Read the original ...

The field of cell and gene therapy has experienced remarkable growth over the last ten years. Autologous and allogeneic therapies have extended their reach across various indications, such as oncology ...

Medical device equipment manufacturers work in an environment where product quality isn't just a competitive advantage, it's a regulatory necessity with direct implications for patient safety. As ...

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Validation ensures that a part will operate correctly in end-user applications. Design validation is the task of testing a part or a system adequately to ensure that all parts or systems manufactured ...

The rigorous testing and validation of web services and APIs is pivotal in ensuring robust integration, security and reliability in today’s networked software systems. With the increasing adoption of ...