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Volumn 36, Issue 2, 2002, Pages 465-480

Will data privacy impact health research?

Author keywords

Data privacy; Directive 95 46 EC; European Community

Indexed keywords

CONFERENCE PAPER; EUROPEAN UNION; GENETICS; GENOMICS; INFORMATION PROCESSING; LAW; LICENSING; MEDICAL ETHICS; MEDICAL RESEARCH; PHARMACOGENOMICS; PRIORITY JOURNAL; PRIVACY; VALIDATION PROCESS;

EID: 0036374943     PISSN: 00928615     EISSN: None     Source Type: Journal    
DOI: 10.1177/009286150203600227     Document Type: Conference Paper
Times cited : (1)

References (4)
  • 1
    • 0010379220 scopus 로고    scopus 로고
    • European Community. Directive 95/46/EC of the European Parliament and the Council of 24 October 1995 on the protection of individuals with regard to the processing of personal data and on the free movement of such data. Brussels, Belgium: European Community Commission; 1995
    • European Community. Directive 95/46/EC of the European Parliament and the Council of 24 October 1995 on the protection of individuals with regard to the processing of personal data and on the free movement of such data. Brussels, Belgium: European Community Commission; 1995.
  • 2
    • 0035962322 scopus 로고    scopus 로고
    • The promise of human genetic data-bases. High ethical as well as scientific standards are needed
    • Lowrance WW. The promise of human genetic data-bases. High ethical as well as scientific standards are needed. Br Med J. 2001;322(7293):1009-1010.
    • (2001) Br Med J , vol.322 , Issue.7293 , pp. 1009-1010
    • Lowrance, W.W.1
  • 3
    • 0033806483 scopus 로고    scopus 로고
    • Regulatory aspects of the application of pharmacogenetics in drug discovery and development in Europe
    • Knudsen LE, Renneberg J. Regulatory aspects of the application of pharmacogenetics in drug discovery and development in Europe. Good Clin Pract. 2000; 7(6):11-13.
    • (2000) Good Clin Pract , vol.7 , Issue.6 , pp. 11-13
    • Knudsen, L.E.1    Renneberg, J.2
  • 4
    • 0010334847 scopus 로고    scopus 로고
    • Regulatory requirements for inclusion of pharmacogenetic testing in applications for clinical trials in Europe
    • Theilade MD, Ehlert Knudsen L, Renneberg J. Regulatory requirements for inclusion of pharmacogenetic testing in applications for clinical trials in Europe. Regulatory Aff J. 2001;12(2):92-99.
    • (2001) Regulatory Aff J , vol.12 , Issue.2 , pp. 92-99
    • Theilade, M.D.1    Ehlert Knudsen, L.2    Renneberg, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.