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USP Chapter 41 Weighing Requirements on Balances in Pharmceutical Quality Control
USP Chapter 41 weighing requirements are mandatory in a Pharmaceutical Quality Control laboratory, where weighing is a fundamental step.
Perspective of Aseptic Sampling
Microbial control is a major objective for all sterile drug manufacturers, with bioburden reduction representing a significant share of risk mitigation efforts
100% traceability in compliance with GLP and accredited procedures
Reference samples, called standards, are required to determine the concentration of chemical compounds using highly sensitive quantitative analytical procedures
Download information to see your options, including suggested alternatives to NPEs and OPEs
It’s time to act if you are using alkylphenol ethoxylate (APE) surfactants such as nonylphenol ethoxylates (NPEs) and octylphenol ethoxylates (OPEs)
Simulated moving bed chromatography (SMBC) for higher productivity and significantly lower costs
Simulated moving bed chromatography (SMBC) is an HPLC technique that continuously separates substance mixtures and extracts them into two fractions
POC diagnosis: Compact multispectral sensor delivers fast, medically specific test results
Learn how the multispectral PixelSensor™ is revolutionizing sophisticated point-of-care testing in healthcare
The experiment shown here illustrates how thermal and colloidal stability can be measured simultaneously
This article highlights a study demonstrating the benefits of FFF-MALS-DLS for the char- acterization of nanolipid particles