Osmolality is a well-established parameter for upstream bioprocessing, formulation, analytical development and QC applications throughout the manufacturing of biological drugs. A recent publication ...

DOVER, DE, UNITED STATES, January 21, 2026 /EINPresswire.com/ -- The global pharmaceutical supply chain is currently ...

Pharmaceutical manufacturing and quality control processes are stuck in the past. Process Analytical Technology (PAT) can bring production systems up-to-date and help realize manufacturing efficiency ...

Optimizing the downstream process for adeno-associated virus (AAV) production with consistent quality depends on the ability to characterize critical quality attributes affecting the final product’s ...

Dr. Hager: A significant development in bioprocessing has been the ability to increase titers across a variety of cell types and protein types. When biologics manufacturing was in its infancy, there ...

Data integrity, impurity characterization, and stability requirements are key focus areas in drug substance testing, with advanced analytical technologies enhancing accuracy. Newer modalities, ...

Biopharma quality control is being revolutionized by advanced analytics and digital transformation through a synergy that boosts quality and scalability. *Full transcript available below. Digital ...

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The Thermo Scientific™ MarqMetrix™ All-In-One Process Raman Analyzer is a compact, powerful solution for continuous Process Analytical Technology (PAT) monitoring across both upstream and downstream ...