General method validation guidelines for pharmaceutical samples

J Chromatogr Sci. 1987 Jun;25(6):252-6. doi: 10.1093/chromsci/25.6.252.

Abstract

Method validation guidelines, which provide an organizational structure for the design and evaluation of a validation procedure, are presented for a wide range of pharmaceutical applications. The validation guidelines are based on the analyte concentration/sample matrix combination to which the method will be applied. These guidelines include the selection of appropriate validation parameters, design considerations for evaluation, and a discussion of acceptance guidelines for the determination of acceptable method performance. A set of tables is included which illustrates the selection and testing procedure and tailors the entire validation process to the specific characteristics of the determination to be made.

MeSH terms

  • Chemistry, Pharmaceutical
  • Drug Stability
  • Pharmaceutical Preparations / analysis*
  • Reference Standards

Substances

  • Pharmaceutical Preparations