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High-Throughput Analysis of Volatile Impurities in Sustainable Packaging using SIFT-MS Automated Sample Prep in Regulated and Nonregulated Labs Just Got Easier What is Chemical Composition Distribution in Polyolefins, and Why Should It Be Part of Your HT GPC Analysis?How Well Do You Pipette?Probe Electrospray Ionization-Mass Spectrometry and Isotope Dilution Approaches

High-Throughput Analysis of Volatile Impurities in Sustainable Packaging using SIFT-MSAutomated Sample Prep in Regulated and Nonregulated Labs Just Got EasierWhat is Chemical Composition Distribution in Polyolefins, and Why Should It Be Part of Your HT GPC Analysis?How Well Do You Pipette?Probe Electrospray Ionization-Mass Spectrometry and Isotope Dilution Approaches

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View More Liquid Chromatography (LC/HPLC)Gas Chromatography (GC)Sample Preparation Mass Spectrometry Pharmaceutical Analysis Environmental Analysis Food and Beverage Analysis

Liquid Chromatography (LC/HPLC)Gas Chromatography (GC)Sample PreparationMass SpectrometryPharmaceutical AnalysisEnvironmental AnalysisFood and Beverage Analysis

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All App NotesBiological, Medical, and ClinicalBiopharmaceuticalsCannabisChiralEnvironmentalFood and BeverageGCGC-MSGeneralIndustrialLCLC-MSMedical/BiologicalMisc TechniquesPharmaceuticalsPolymersSample PrepSize-Exclusion Chromatography (SEC)Supercritical Fluid Chromatography (SFC)

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Articles

LCGC North America

Current Practices and Considerations for a Stability-Indicating Method in Pharmaceutical Analysis

What are the characteristics and relevant considerations for the development and validation of a stability-indicating method?

LCGC Europe

Current Practices and Considerations for a Stability-Indicating Method in Pharmaceutical Analysis

In the pharmaceutical industry, the demonstration of drug substance (DS) or drug product (DP) stability over the shelf life is an important aspect of the regulatory requirements.