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Zdrowie i gospodarka · 9/13/2013

Draft Guidance for Industry on Bioanalytical Method Validation; Availability

The Food and Drug Administration (FDA) is announcing the availability of a draft guidance for industry entitled "Bioanalytical Method Validation." The draft guidance is intended to provide recommendations regarding analytical method development and validation for the measurement of drugs and/or metabolites, therapeutic biologics, and biomarkers for sponsors of investigational new drug applications (INDs), new drug applications (NDAs), abbreviated new drug applications (ANDAs), and biologics license applications (BLAs) for therapeutic biologics regulated by the Center for Drug Evaluation and Research. This draft guidance may apply to some studies related to the veterinary drug approval process (Investigational New Animal Drugs (INADs), New Animal Drug Applications (NADAs), and Abbreviated New Animal Drug Applications (ANADAs)) regulated by the Center for Veterinary Medicine. This guidance was originally issued in 2001. FDA is revising the guidance to reflect advancements in the science and technology of bioanalytical method validation.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →