Testing is a key part of any product development cycle. Done right, it turns up unknown bugs and problems, and allows for them to be fixed prior to shipment. However, it can be a costly and ...

A simple procedure accurately characterizes reservoir fluids for designing oil and gas production facilities without significant compromise. The procedure involves defining a small number of ...

Matt Taylor is a senior process development associate at KBI Biopharma, where he focuses on the design, optimization, and scale-up of purification processes for biopharmaceutical manufacturing. Matt ...

This white paper offers concise, practical guidance for biopharma teams outsourcing Process Characterization (PC) to strengthen CMC packages and accelerate commercialization. Get the essential updates ...

Process validation plays a critical role in the success for a new biopharmaceutical on the path of commercialization, including the crucial process characterization. As a program advances towards ...

Quantum process characterization encompasses a suite of diagnostic methods that quantify and reconstruct the transformation enacted by quantum hardware on qubits. As devices scale beyond a handful of ...

Every new SoC tape-out demands broader coverage for design robustness, and the characterization workload has exploded. The ...

Solido Simulation Suite’s purpose-built library IP simulator Solido LibSPICE provides an additional 2x+ boost. New AI-powered ...

Process validation, including process characterization, is a critical step in the successful commercialization of a new biopharmaceutical on its path to commercialization. As the program approaches ...

Process characterization and viral clearance validation are pivotal studies in biopharmaceutical manufacturing, particularly for monoclonal antibodies (mAbs) produced in mammalian systems, which carry ...