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Zdrowie i gospodarka · 07/03/1996

International Conference on Harmonisation; Draft Guideline on the Validation of Analytical Procedures: Methodology; Availability

The Food and Drug Administration (FDA) is publishing a draft guideline entitled ``Validation of Analytical Procedures: Methodology.'' The draft guideline was prepared under the auspices of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). The draft guideline provides recommendations on how to consider various validation characteristics for each analytical procedure. The draft guideline is an extension to the ICH guideline entitled ``Text on Validation of Analytical Procedures.''

Source: Federal Register — Food and Drug AdministrationOpen original release →