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 ...

Market opportunities lie in enhancing risk-based V&V planning, focusing on DQ, IQ, OQ, and PQs to address cGMP deficiencies and regulatory expectations. By aligning with FDA, ICH, and ISO standards, ...

From my product development experiences, entering into Design Verification and Design Validation is always bittersweet. Exciting because yes, to get to Design Verification means that we have ...

While often used intermixed, verification and validation are quite different procedures with different goals and different means to achieve those goals. No better way to clear up the confusion by ...

The ISO 16140-1:2016 standard for the validation of alternative (proprietary) microbiological methods provides a specific protocol and guidelines. Jun 24, 2016 ISO announced that the ISO 16140:2003 ...

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 ...

Every product has defects. Finding them as early in the development process as possible is definitely something to strive for. Building quality into software as it's being developed is far more ...

Computational models and simulations have had an important role in engineering analysis since as far back as the 1960s. It is widely recognized that the use of modeling and simulation tools can make ...

A key focus of the IC design industry is to deliver first-pass silicon, which means finding most, if not all, of the potential defects before tape-out. This is extremely difficult due to increasing ...