The Quality Assurance JournalVolume 3, Issue 4 p. 153-207 Research ArticleFree Access Guide for auditing manufacturing of active pharmaceutical ingredients for clinical trials1 Good Manufacturing Practice Committee of the French Society of Quality Assurance, Good Manufacturing Practice Committee of the French Society of Quality AssuranceSearch for more papers by this author Good Manufacturing Practice Committee of the French Society of Quality Assurance, Good Manufacturing Practice Committee of the French Society of Quality AssuranceSearch for more papers by this author First published: 22 June 2000 https://doi.org/10.1002/1099-1786(199812)3:4<153::AID-QAJ77>3.0.CO;2-C 1 This document was originally published in French by the French Society of Quality Assurance (SOFAQ) under the title ‘Guide d'Audit de la Fabrication des Principes Actifs destinés aux Essais Cliniques’ (September 1998). Special thanks are due to Ray Lowing and Bernard Dreyer for their help in reviewing the English language version. AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Volume3, Issue4December 1998Pages 153-207 ReferencesRelatedInformation