Research Articles
Quantitation of Class 1, 2, and 3 Residual Solvents: A Comprehensive Guide for Pharmaceutical Analysis
This article provides a comprehensive overview of the quantitation of residual solvents, essential for ensuring the safety and quality of pharmaceuticals.
Automated Headspace Sampling in Pharmaceutical QC: Enhancing Accuracy, Efficiency, and Compliance
This article provides a comprehensive overview of automated headspace sampling technology and its critical role in modern pharmaceutical quality control.
DB-FFAP Column for Residual Solvents Analysis: A Comprehensive Guide from Method Development to Validation
This article provides a complete resource for researchers and pharmaceutical analysis professionals on utilizing the DB-FFAP gas chromatography column for residual solvents testing.
Development and Validation of a Static Headspace GC-FID Method for Residual Solvent Analysis in Linezolid Active Substance
This article details the development, optimization, and validation of a static headspace gas chromatography with flame ionization detection (HS-GC-FID) method for the determination of seven residual solvents in the linezolid...
Residual Solvents in Liposomes and Nanomedicine: Analysis, Challenges, and Regulatory Compliance
This article provides a comprehensive overview of residual solvent analysis in liposome and nanomedicine formulations, addressing critical needs for researchers and drug development professionals.
Developing a Universal GC-FID Method with Hydrogen Carrier Gas for High-Throughput Analysis of 30+ Residual Solvents
This article presents a comprehensive guide to developing, optimizing, and validating a generic Gas Chromatography-Flame Ionization Detection (GC-FID) method using hydrogen as a carrier gas for the simultaneous analysis of...
Elite-624 GC Column Method for Pharmaceutical Residual Solvent Analysis: A Complete Guide from Method Development to Validation
This comprehensive guide details the application of the Elite-624 GC column for the analysis of residual solvents in pharmaceuticals, aligning with ICH Q3C guidelines.
Optimizing Nanoformulation Analysis: A Complete Guide to PerkinElmer Headspace GC-FID Setup and Method Validation
This article provides a comprehensive guide for researchers and drug development professionals on implementing PerkinElmer Headspace GC-FID systems for analyzing residual solvents and volatile compounds in nanoformulations.
Residual Solvent Analysis in Pharmaceuticals: A 2025 Guide to Regulatory Requirements, Methods, and Compliance
This article provides drug development scientists and regulatory affairs professionals with a comprehensive guide to the current landscape of residual solvent analysis.
A Robust Static Headspace GC-FID Method for the Analysis of 13 Residual Solvents: Development, Optimization, and Validation for Pharmaceutical Applications
This article provides a comprehensive guide for researchers and drug development professionals on developing, optimizing, and validating a static headspace gas chromatography with flame ionization detection (HS-GC-FID) method for the...