PFAS in Pharmaceuticals: An Evolving Regulatory Landscape
Examine the regulatory crossroads resulting from the ubiquitous presence of PFAS in widely prescribed drugs.
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Examine the regulatory crossroads resulting from the ubiquitous presence of PFAS in widely prescribed drugs.
Learn about the purification of single-stranded RNA oligonucleotides by ion-pair reversed-phase chromatography.
A GC-MS method to determine nitrosamines in Valsartan tablets according to US FDA guidelines is described.
Discover an effective method for drug quantitation in biological fluids, a high-throughput analysis for simple fractionation and more...
COVID-19: Simultaneous Analysis of Remdesivir and Metabolites in Human Plasma Using Fully Automated Sample Preparation LC/MS/MS System and Fully Automated Quantification of Meropenem, Tazobactam, Piperacillin and Dexamethasone...
Mr. Rich Youn explains the need for the scientific community to support each other for tomorrow’s Pharma 4.0 environment.
Discover the vital role of compendial methods in pharmaceutical analysis and how to make adjustments to them for HPLC separations
Discover the importance of AF4 and light scattering in the study of protein aggregation.
Discover how light scattering with size-exclusion chromatography can help in your polymer analytical characterization.
In this study, an immunoaffinity high resolution accurate mass (HRAMS) assay is presented as a complementary analytical technique for signature peptide quantification. The assay performance is measured...
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