The FDA recently updated its 1987 guidelines for submitting samples and analytical data for method validation — a document that affects all analytical chemists working in the pharmacrutical industry. This article highlights the agency's recommendations of how to report and validate analytical data in all new drug applications.
The FDA recently updated its 1987 guidelines for submitting samples and analytical data for method validation — a document that affects all analytical chemists working in the pharmacrutical industry. This article highlights the agency's recommendations of how to report and validate analytical data in all new drug applications.
This article examines the role that multidimensional chromatography systems will play in high-throughput proteomics.
This article examines the role that multidimensional chromatography systems will play in high-throughput proteomics.
Norberto Guzman and Ron Majors look at three areas in which progress has been made in improving concentration limits of detection for CE and CE microchip techniques: preconcentration methods, detector enhancements, and derivatization methods to improve separation selectivity and to enhance detection.
The FDA recently updated its 1987 guidelines for submitting samples and analytical data for method validation — a document that affects all analytical chemists working in the pharmacrutical industry. This article highlights the agency's recommendations of how to report and validate analytical data in all new drug applications.
The FDA recently updated its 1987 guidelines for submitting samples and analytical data for method validation — a document that affects all analytical chemists working in the pharmacrutical industry. This article highlights the agency's recommendations of how to report and validate analytical data in all new drug applications.
The FDA recently updated its 1987 guidelines for submitting samples and analytical data for method validation — a document that affects all analytical chemists working in the pharmacrutical industry. This article highlights the agency's recommendations of how to report and validate analytical data in all new drug applications.
The authors focus on problems that may occur when converting conventional methods to LC–MS.
The FDA recently updated its 1987 guidelines for submitting samples and analytical data for method validation — a document that affects all analytical chemists working in the pharmacrutical industry. This article highlights the agency's recommendations of how to report and validate analytical data in all new drug applications.
The FDA recently updated its 1987 guidelines for submitting samples and analytical data for method validation — a document that affects all analytical chemists working in the pharmacrutical industry. This article highlights the agency's recommendations of how to report and validate analytical data in all new drug applications.
Guest author Barry Lesnik attempts to clarify the multiple uses of the term validation in environmental analysis.
This installment of "Directions in Discovery" describes experiments performed to optimize a standard quality-control method for protein purity evaluation using reducing capillary gel electrophoresis.
This article examines the role that multidimensional chromatography systems will play in high-throughput proteomics.
This installment of "Directions in Discovery" describes experiments performed to optimize a standard quality-control method for protein purity evaluation using reducing capillary gel electrophoresis.
The FDA recently updated its 1987 guidelines for submitting samples and analytical data for method validation — a document that affects all analytical chemists working in the pharmacrutical industry. This article highlights the agency's recommendations of how to report and validate analytical data in all new drug applications.
The FDA recently updated its 1987 guidelines for submitting samples and analytical data for method validation — a document that affects all analytical chemists working in the pharmacrutical industry. This article highlights the agency's recommendations of how to report and validate analytical data in all new drug applications.
This month's column looks at methods for preparing calibration standards for VOC analysis.
Part II of this series describes different ways electrolytes can be buffered while maintaining compatibility with indirect detection.
This article examines the role that multidimensional chromatography systems will play in high-throughput proteomics.
This article examines the role that multidimensional chromatography systems will play in high-throughput proteomics.
This article describes a case study in which forensic chemical analyses were conducted to determine the liability for the release of an unknown petroleum product into a river.
This article describes a case study in which forensic chemical analyses were conducted to determine the liability for the release of an unknown petroleum product into a river.
The authors discuss two environmental applications for accelerated solvent extraction.
This article describes a case study in which forensic chemical analyses were conducted to determine the liability for the release of an unknown petroleum product into a river.
A high performance thin-layer chromatographic (HPTLC) method was developed for the determination of aflatoxin B1 in cereals.
This month's installment illustrates some potential problems that may arise during method transfer.
The authors describe two tests performed using SPE. The first involved sterol isolation and cleanup of seed oils, and the second analyzed crude seed oils.
The authors describe two tests performed using SPE. The first involved sterol isolation and cleanup of seed oils, and the second analyzed crude seed oils.
This column discusses the activities of a Russian pioneer of GC and outlines the principles of some of the techniques he developed.