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 ...

Contract manufacturers have special expertise in the characterization and validation of biopharmaceutical manufacturing processes. Process development is a key factor in the development and ...

Additive manufacturing relies on the precise deposition and consolidation of fine powders to produce complex three-dimensional parts with tailored properties. Central to process performance is the ...

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

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

Today’s semiconductor applications, ranging from advanced sensory applications, IoT, edge computing devices, high performance computing, to dedicated A.I. chips, are constantly pushing the boundaries ...

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