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, ...
DUBLIN--(BUSINESS WIRE)--The "Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)" conference has been added to ...
DUBLIN--(BUSINESS WIRE)--The "Validation, Verification and Transfer of Analytical Methods (Understanding and implementing guidelines from FDA/EMA, USP and ICH)" conference has been added to Research ...
With the increased use of electronics and software in the automotive systems, there are strict requirements for complex functions to perform safely and avoid causing damages to life and property in ...
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 ...
Meeting the quality requirements of a complex SoC requires managing large verification projects. In this article, we recount a recent experience with a verification management solution (Incisive ...
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 ...
As the complexity of integrated circuit (IC) designs continues to rise, the task of verifying these designs has become increasingly challenging. The pace of this growth is staggering, with design ...
Formal methods represent a rigorous suite of mathematical techniques designed to specify, develop and verify system models with a high degree of reliability. In system modelling, these methods provide ...
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