THE VALIDATION CRITERIA FOR ANALYTICAL METHODS USED IN PHARMACY PRACTICE RESEARCH
- 1 December 1989
- journal article
- research article
- Published by Hindawi Limited in Journal of Clinical Pharmacy & Therapeutics
- Vol. 14 (6) , 465-473
- https://doi.org/10.1111/j.1365-2710.1989.tb00272.x
Abstract
An integral part of analytical method development is validation, i.e. once the method has been devised it is necessary to evaluate it under the conditions expected for real samples before being used for a specific purpose. Although the validation stage is crucial in method development, the importance of this step is often overlooked. This paper attempts to clarify the nomencleature of method validation and describes the validation procedure for analytical methods used for the determination of drugs in biological fluids and formulations.This publication has 11 references indexed in Scilit:
- Therapeutic monitoring of free (unbound) drug levels: Analytical aspectsTrAC Trends in Analytical Chemistry, 1989
- HIGH-PERFORMANCE LIQUID CHROMATOGRAPHIC ANALYSIS OF RANITIDINE IN PLASMA AND URINEJournal of Clinical Pharmacy & Therapeutics, 1988
- An overview of contemporary method development in liquid chromatographyChromatographia, 1988
- General Method Validation Guidelines for Pharmaceutical SamplesJournal of Chromatographic Science, 1987
- Rapid high-performance liquid chromatographic method for the determination of propranolol in plasmaThe Analyst, 1987
- Validationof chromatographic methods of analysis of drugs in biological samplesTrAC Trends in Analytical Chemistry, 1986
- Analytical strategies for therapeutic monitoring of drugs in biological fluidsJournal of Chromatography B: Biomedical Sciences and Applications, 1985
- Modern drug analysis in biological fluids suitable for clinical pharmacokineticsJournal of Pharmaceutical and Biomedical Analysis, 1983
- Limits of the internal standard technique in chromatographyJournal of Chromatography A, 1981
- Quality control of prednisolone sodium phosphateThe Analyst, 1980