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

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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 ...

We performed an extensive characterization of an electrospinning process to evaluate how the process parameters and precursor solution characteristics affect the fibers morphology. The work was ...

We recommend using k=51 when searching against eukaryotic genomes, as there seem to be many false positives at smaller ksizes. :::success Note that the entire database used here is NCBI eukaryotes + ...

The biopharmaceutical industry exists to develop novel therapeutics that address unmet medical needs. The evolving research and development landscape for these complex therapeutics has made ...

Antibody-drug conjugates (ADCs) represent an innovative class of potent anti-cancer agents. They combine the specificity of a monoclonal antibody with the potency of a cytotoxic drug, enabling ...

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 ...

Continued scaling of integrated circuits to smaller dimensions is still a viable way to increase compute power, achieve higher memory cell density, or reduce power consumption. These days, chip makers ...

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