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Cannabis Analysis
Capillary Electrophoresis
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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
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LCGC TV: Sample Preparation
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Liquid Chromatography (LC/HPLC)
Market Profiles
Mass Spectrometry
Medical/Biological
Multidimensional GC
Multidimensional LC
Peer-Reviewed Articles
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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
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John D. Orr

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Validation of Impurity Methods, Part II

Michael E. Swartz;Ira S. Krull;John D. Orr
December 1st 2003

Second column in a series that reviews impurity method validation guidelines.

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Validation of Impurity Methods, Part I

Michael E. Swartz;Ira S. Krull;John D. Orr
July 1st 2003

This column is the first installment in a two-part series reviewing ICH and FDA impurity method validation guidelines.

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