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, ...

Market opportunities arise in providing solutions for cGMP software verification and validation, addressing increased FDA scrutiny. Demand exists for expertise in FDA guidelines, risk management ...

When The MathWorks introduced Matlab technical-computing software more than 20 years ago, many of the first users were control-system designers. Anyone who had laboriously inverted matrices by hand to ...

The U.S. Nuclear Regulatory Commission (NRC) issues initial licenses for commercial nuclear power plants for 40 years of operation – a period originally based on economic and antitrust considerations, ...

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 ...

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 ...

When it comes to verification and validation, medical device companies need to ensure that what they're doing actually makes sense. Known colloquially as "V&V," for many it feels like you're on the ...

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 ...

BRAINTREE, Mass., Nov. 13, 2023 (GLOBE NEWSWIRE) -- Microbot Medical Inc. (MBOT), developer of the innovative LIBERTY ® Robotic Surgical System, today announces it had successfully completed the ...