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 ...

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 ...

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, ...

NASA has selected Northrop Grumman Information Technology, Falls Church, Va., and Titan Corporation, Reston, Va. for the Independent Verification and Validation (IV&V) of Software Services. The two ...

Overview: This webinar will give valuable help to FDA regulated Pharmaceutical, Medical Device, Biotech, Diagnostics and Biological manufacturers. In August 2010, FDA made an announcement affecting ...

If chip design had a face, it would have a wrinkle or two, an especially deep one caused by the increasingly complex challenge of hardware and software verification. Until recently, these two elements ...

Apple announced in November the first 16 billion transistor system-on-chip (SoC) design as part of a planned SoC family manufactured on the 5-nm process node. Measured in ASIC equivalent gates, the ...

Verification expert Dr. Lauro Rizzatti debunks the myths surrounding the two tool classes of HAV platforms—hardware emulators and FPGA prototypes. What are hardware emulators and FPGA prototypes? Who ...

Defining what a processor is, and what it is supposed to do, is not always as easy as it sounds. In fact, companies are struggling with the implications of hundreds of heterogenous processing elements ...