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Date: 2006-11-21 08:37:58Pharmaceutical industry Research Pharmaceuticals policy Combination drug Good manufacturing practice Bioequivalence Regulatory requirement Committee for Medicinal Products for Human Use Pharmacovigilance Pharmaceutical sciences Pharmacology Clinical research | This report contains the collective views of an international group of experts and does not necessarily represent the decisions or the stated policy of the World Health Organization WHO Technical Report Series 929Add to Reading ListSource URL: apps.who.intDownload Document from Source WebsiteFile Size: 973,85 KBShare Document on Facebook |
Paste your photo here Paste your Logo here Title: E-BABE-Encyclopedia of Bioanalytical Methods for Bioavailability and Bioequivalence Studies of PharmaceuticalsDocID: 1vrPD - View Document | |
Title: E-BABE-Encyclopedia of Bioanalytical Methods for Bioavailability and Bioequivalence Studies of PharmaceuticalsDocID: 1vrMl - View Document | |
Title: E-BABE-Encyclopedia of Bioanalytical Methods for Bioavailability and Bioequivalence Studies of PharmaceuticalsDocID: 1vk4H - View Document | |
Title: Encyclopedia of Bioanalytical Methods for Bioavailability and Bioequivalence Studies of PharmaceuticalsDocID: 1viUy - View Document | |
Title: E-BABE-Encyclopedia of Bioanalytical Methods for Bioavailability and Bioequivalence Studies of PharmaceuticalsDocID: 1viBz - View Document |