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Volumn 45, Issue 7, 2007, Pages 843-850

Third Santorini conference pharmacogenomics workshop report: "Pharmacogenomics at the crossroads: What else than good science will be needed for the field to become part of Personalized Medicine?"

(19)  Llerena, Adrián a   Michel, Gerd b   Jeannesson, Elise c   Wong, Steven d   Manolopoulos, Vangelis G e   Hockett, Richard Dean f   Boubekeur, Karima g   Siest, Gérard h   Beaune, Philippe i   Haefliger, Carolina j   Arnold, Hans Peter k   Junien, Claudine l   Petrovic, Nenad m   Molloy, Roisin n   Bekers, Otto o   Donnelly, Claudine n   Arens, Hans Juergen p   Kaput, Jim q   McComb, Joel r  


Author keywords

Education; Industry; Personalized Medicine; Pharmacogenomics; Regulatory aspects

Indexed keywords

CLINICAL PRACTICE; CONFERENCE PAPER; COST EFFECTIVENESS ANALYSIS; DRUG INDUSTRY; DRUG SCREENING; FOOD AND DRUG ADMINISTRATION; HUMAN; KNOWLEDGE; MEDICAL EDUCATION; MEDICAL LITERATURE; MEDICAL RESEARCH; NONHUMAN; ORGANIZATION AND MANAGEMENT; PHARMACOGENOMICS; PRIORITY JOURNAL; SOCIOECONOMICS;

EID: 34447274216     PISSN: 14346621     EISSN: 14374331     Source Type: Journal    
DOI: 10.1515/CCLM.2007.182     Document Type: Conference Paper
Times cited : (7)

References (10)
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    • Pharmacogenomics education: International Society of Pharmacogenomics recommendations for medical, pharmaceutical, and health schools deans of education
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    • Gurwitz, D.1    Lunshof, J.E.2    Dedoussis, G.3    Flordellis, C.S.4    Fuhr, U.5    Kirchheiner, J.6
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    • National Academy of Clinical Biochemistry, analysis and application of pharmacogenetics to clinical practice
    • National Academy of Clinical Biochemistry. Laboratory guidelines and recommendations for laboratory analysis and application of pharmacogenetics to clinical practice. http://www.aacc.org/NR/rdonlyres/AE772314-08C0-4F75-9895- D40B7181E4F8/0/LMPG_Pharmacogenetics.pdf.
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    • Experience with voluntary and required genomic data submissions to the FDA: Summary report from track 1 of the third FDA-DIA-PWG-PhRMA-BIO pharmacogenomics workshop
    • Frueh FW, Rudman A, Simon K, Gutman S, Reed C, Dorner AJ. Experience with voluntary and required genomic data submissions to the FDA: summary report from track 1 of the third FDA-DIA-PWG-PhRMA-BIO pharmacogenomics workshop. Pharmacogenomics J 2006;6:296-300.
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    • The drug diagnostic co-development concept paper: Commentary from the 3rd FDA-DIA-PWG-PhRMA-BIO Pharmacogenomics Workshop
    • Hinman LM, Huang SM, Hackett J, Koch WH, Love PY, Pennello G, et al. The drug diagnostic co-development concept paper: commentary from the 3rd FDA-DIA-PWG-PhRMA-BIO Pharmacogenomics Workshop. Pharmacogenomics J 2006;6:375-80.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.