Pharmacogenomic data submissions to the FDA: clinical pharmacology case studies
| Autor: | Roberto Guerciolini, Andrew J Dorner, Gualberto Ruaño, Shiew-Mei Huang, Jerry M. Collins, Sue-Jane Wang |
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| Rok vydání: | 2004 |
| Předmět: | |
| Zdroj: | Pharmacogenomics. 5:513-517 |
| ISSN: | 1744-8042 1462-2416 |
| Popis: | Gualberto Ruano1,2, Jerry M Collins3, Andrew J Dorner4, Sue-Jane Wang5, Roberto Guerciolini6 & Shiew-Mei Huang†7 †Author for correspondence 1President, Genomas LLC, New Haven, CT, USA 2Department of Biochemistry and Molecular Biology, George Washington University, Washington DC, USA 3Director, Laboratory of Clinical Pharmacology, CDER, FDA, USA 4Senior Director, Molecular Medicine, Wyeth Research 5Lead Senior Mathematical Statistician, FDA, InterCenter Pharmacogenomics/ Pharmacogenetics Initiative, USA 6Senior Director, Millennium Pharmaceuticals, Inc., USA 7Deputy Office Director for Science, Office of Clinical Pharmacology and Biopharmaceutics, HFD-850, Center for Drug Evaluation and Research, FDA, 5600 Fishers Lane, PKLN 6A/19, Rockville, MD 20850, USA E-mail: huangs @cder.fda.gov |
| Databáze: | OpenAIRE |
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