Introduction In the realm of pharmaceutical manufacturing and chemical synthesis, the identification and monitoring of in-process organic compounds are critical […]
Identification of In-Process Organic Compounds using LCMS Read More »
Introduction The development and submission of generic drugs to the U.S. Food and Drug Administration (USFDA) involves stringent regulatory requirements
Impurity Profiling and Characterization for Generic Project Submission to USFDA Read More »
Introduction In recent years, the presence of nitrosamine impurities in pharmaceuticals has become a significant concern for regulatory agencies and
Nitrosamine Impurities Testing Read More »
ResolveMass Laboratories Inc. Introduces Advanced Mass Spectrometry Capabilities ResolveMass Laboratories Inc. announces a significant enhancement in its analytical capabilities with
ResolveMass Laboratories Inc. Introduces Advanced Mass Spectrometry Capabilities Read More »
