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Volumn 173, Issue 2, 2004, Pages 72-74

Ethical approval for national studies in Ireland: An illustration of current challenges

Author keywords

[No Author keywords available]

Indexed keywords

ACUTE DISEASE; ARTICLE; CLINICAL STUDY; HEALTH CARE FINANCING; HEALTH CARE ORGANIZATION; HEALTH CENTER; HEALTH SERVICES RESEARCH; HEALTH SURVEY; HEART MUSCLE ISCHEMIA; HOSPITAL MANAGEMENT; HOSPITAL PERSONNEL; HUMAN; INFORMATION PROCESSING; INTENSIVE CARE UNIT; IRELAND; MEDICAL DOCUMENTATION; MEDICAL ETHICS; ORGAN DONOR; OUTCOMES RESEARCH; QUESTIONNAIRE;

EID: 7244239209     PISSN: 00211265     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF02914559     Document Type: Article
Times cited : (9)

References (3)
  • 1
    • 85039496726 scopus 로고    scopus 로고
    • From Medical Biotechnology to Clinical Practice - Report of a Workshop organised under the aegis of the Cell Factory Key Action
    • External Advisory Group (EAG) of the Cell Factory Key Action. Quality of Life Programme, European Commission, Research Directorate General, Brussels
    • External Advisory Group (EAG) of the Cell Factory Key Action. From Medical Biotechnology to Clinical Practice - Report of a Workshop organised under the aegis of the Cell Factory Key Action. Quality of Life Programme, European Commission, Research Directorate General, Brussels, 2000.
    • (2000)
  • 2
    • 0003177157 scopus 로고    scopus 로고
    • Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use
    • Official Journal of the European Communities (accessed 13 January, 2004)
    • Directive 2001/20/EC of the European Parliament and of the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use. Official Journal of the European Communities 2001; L121: 34-44 http://europa.eu.int/eur-lex/en/archive/2001/1_12120010501en.html (accessed 13 January, 2004).
    • (2001) , vol.L121 , pp. 34-44
  • 3
    • 0037129618 scopus 로고    scopus 로고
    • Implications of the EU directive on clinical trials for emergency medicine
    • Singer EA, Mullner M. Implications of the EU directive on clinical trials for emergency medicine. BMJ 2002; 324: 1169-70.
    • (2002) BMJ , vol.324 , pp. 1169-1170
    • Singer, E.A.1    Mullner, M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.