News|Articles|June 29, 2026
Managing bias in LC-UV potency assays
Author(s)LGC Standards
Potency testing workflows and key factors affecting quantitative accuracy, with a case study led guide to producing reliable, defensible data.
Related Content
- Analytical Instrumentation
- Analytical Theory
- Biological, Medical, and Clinical Analysis
- Biopharmaceutical Perspectives
- Biopharmaceuticals and Protein Analysis
- Cannabis Analysis
- Capillary Electrophoresis
- Chiral Chromatography
- ChromAcademy
- Corporate Profiles
- Data Acquisition, Handling, and Archiving
- Data Analysis, Statistics, and Chemometrics
- Dietary Supplements Analysis
- Environmental Analysis
- Field-Flow Fractionation (FFF)
- Food and Beverage Analysis
- Forensics, Narcotics
- From the Editor
- GC–MS
- Gas Chromatography (GC)
- HILIC
- HPLC
- Ion Chromatography
- LCGC Interviews
- LCGC TV: Gas Chromatography
- LCGC TV: Hyphenated Techniques
- LCGC TV: Liquid Chromatography
- LCGC TV: Sample Preparation
- LC–MS
- Liquid Chromatography (LC/HPLC)
- Market Profiles
- Mass Spectrometry
- Medical/Biological
- Multidimensional GC
- Multidimensional LC
- Peer-Reviewed Articles
- Pharmaceutical Analysis
- Preparative-Scale Chromatography
- Process Analytical Technology (PAT)
- Quality Control/Quality Assurance (QA/QC)
- Quality by Design (QbD)
- Regulatory Standards, GLP and GMP Compliance
- Sample Preparation
- Size-Exclusion Chromatography (SEC)
- Solid-Phase Extraction (SPE)
- Supercritical Fluid Chromatography (SFC)
- Supercritical Fluid Extraction (SFC)
- The Next Generation
- Thin Layer Chromatography
- Trends
- UHPLC
- Web of Science