Examine the regulatory crossroads resulting from the ubiquitous presence of PFAS in widely prescribed drugs.
Learn about intriguing findings from work with USP Chapter <1469>, Procedure 1, and a successful implementation of Procedure 3.
A thorough look at the contents of GAMP 5 Version 2 release to examine what has changed since the Version 1 release.
Learn about how USP <1058> aligns with GAMP® 5, the core elements of the <1058> instrument life-cycle framework, and areas of <1058> the USP are exploring improvements.
eBook highlighting a variety of applications related to the pharmaceutical and food and beverage markets, specifically highlighting the capabilities of a compact, yet powerful LC-MS system
Learn about the purification of single-stranded RNA oligonucleotides by ion-pair reversed-phase chromatography.
Discover solutions for tackling the most difficult HPLC polar compound analyses using a variety of food and pharma applications
Learn more about the risk assessment and analytical challenges of detection and quantification of trace level impurities in pharmaceuticals.
Detection and Quantification Challenges of Trace Level Impurities in Pharmaceutical Products – Mutagenic Nitrosamines and Beyond
This on-demand discussion forum covers the risk assessment and analytical challenges of detection and quantification of trace level impurities in pharmaceutical products.
A GC-MS method to determine nitrosamines in Valsartan tablets according to US FDA guidelines is described.
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