Search results for " analytical"

Article Host-Cell Protein Measurement and Control
FDA expects “Whenever possible, contaminants introduced by the recovery and purification process should be below detectable levels using a highly sensitive analytical method” (7). The European Medicin…

Article Quality by Design and Extractable and Leachable Testing
These extracted chemicals are then identified by various analytical techniques, typically inductively coupled plasma mass spectrometry (ICP—MS), liquid chromatography-mass spectrometry (HPLC–MS), and …

Article Q&As with Industry Leaders
…vity  Jeanne Linke Northrop, Biopharm International Mary Szorik, Senior Manager of Analytical Services, Cytiva Alice Elwood, Analytical Services Product Manager, Cytiva Chro…

Article Climate Change in Outsourcing
Strategic partnering opportunities in analytical services, clinical trial materials (CTM) manufacturing and clinical supplies management are still in their early stages, and the larger analytical labs…

Article QbD and PAT in Upstream and Downstream Processing
As a result of major advancements in analytical science, direct measurements of CQAs are performed in bioprocessing today. These would be product-quality related parameters, including host-cell impuri…

Article Quality by design for biotechnology products—part 1
Thus, to implement QbD, it is critical to have a fundamental understanding of the functional relationships between patient needs, product quality attributes, analytical capabilities, and the manufactu…

Article Top Process Development Trends for 2022 and a Look into 2023
FDA approved 37 drugs in 2022, within the normal range for the past decade or so. The European Medicines Agency (EMA) was even more successful—approving a record 55 therapies. More than half of thes…

Article Report from the 12th Plasma Product Biotechnology Forum
The general trend was considered more interesting than specific values predicted, as scale-up and variability of analytical methods were not considered. Another aspect of technical development …

Article Pandemic Alters Policies and Practices for Drug Development and Regulation
Interest rose in innovative clinical research methods, such as master protocols, adaptive trial designs, and Bayesian analytical methods to reduce study size and duration. Digital technology was adopt…

Article Single-Use Technologies Prove Effective for Viral Vector Process Development
The company’s Accelerator Process Development Services group can, she says, provide robust industrial-scale processes, including the development of a process analytical technology (PAT) approach, in s…

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