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Date: 2006-11-21 08:38:02Pharmaceutical sciences Pharmaceutics Pharmaceuticals policy Food and Drug Administration Pharmacology Clinical trial Bioequivalence Good Laboratory Practice Good Clinical Practice Clinical research Research Pharmaceutical industry | © World Health Organization WHO Technical Report Series, No. 937, 2006 Annex 9 Additional guidance for organizations performing in vivo bioequivalence studiesAdd to Reading ListSource URL: apps.who.intDownload Document from Source WebsiteFile Size: 371,28 KBShare Document on Facebook |
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