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Volumn 6, Issue 5, 2009, Pages 446-454

The automation of clinical trial serious adverse event reporting workflow

Author keywords

[No Author keywords available]

Indexed keywords

ACCESS TO INFORMATION; ARTICLE; AUTOMATION; CLINICAL STUDY; COMPUTER PROGRAM; DATA ANALYSIS; DATA BASE; DRUG SURVEILLANCE PROGRAM; E-MAIL; PRIORITY JOURNAL; WEB BROWSER;

EID: 71049174486     PISSN: 17407745     EISSN: 17407753     Source Type: Journal    
DOI: 10.1177/1740774509344778     Document Type: Article
Times cited : (8)

References (14)
  • 1
    • 0032944688 scopus 로고    scopus 로고
    • Use of computer-based records, completeness of documentation, and appropriateness of documented clinical decisions
    • Tang PC, LaRosa MP, Gorden SM Use of computer-based records, completeness of documentation, and appropriateness of documented clinical decisions. J Am Med Inform Assoc 1999; 6: 245-51.
    • (1999) J Am Med Inform Assoc , vol.6 , pp. 245-251
    • Tang, P.C.1    LaRosa, M.P.2    Gorden, S.M.3
  • 2
    • 33847024874 scopus 로고    scopus 로고
    • Integrating incident reporting into an electronic patient record system
    • Haller G., Myles PS, Stoelwinder J. et al. Integrating incident reporting into an electronic patient record system. J Am Med Inform Assoc 2007; 14: 175-81.
    • (2007) J Am Med Inform Assoc , vol.14 , pp. 175-181
    • Haller, G.1    Myles, P.S.2    Stoelwinder, J.3
  • 5
    • 33745366190 scopus 로고    scopus 로고
    • Managing the life cycle of electronic clinical documents
    • (Jul-Aug):
    • Payne TH, Graham G. Managing the life cycle of electronic clinical documents. J Am Med Inform Assoc 2006; 13(Jul-Aug): 438-45.
    • (2006) J Am Med Inform Assoc , vol.13 , pp. 438-445
    • Payne, T.H.1    Graham, G.2
  • 7
    • 71049183636 scopus 로고    scopus 로고
    • Title 21 Code of Federal Regulations (21 CFR Part 11) for Electronic Records and Electronic Signatures
    • Title 21 Code of Federal Regulations (21 CFR Part 11) for Electronic Records and Electronic Signatures.
  • 8
    • 71049193554 scopus 로고    scopus 로고
    • Available at: (accessed 4 February 2009)
    • caBIG Core Concepts. Available at: http://cabig.nci.nih.gov/ overview/caBIG_core_concepts (accessed 4 February 2009).
    • CaBIG Core Concepts
  • 9
    • 0035819858 scopus 로고    scopus 로고
    • Monitoring and ensuring safety during clinical research
    • Morse MA, Califf RM, Sugarman J. Monitoring and ensuring safety during clinical research. JAMA 2001; 285: 1201-05.
    • (2001) JAMA , vol.285 , pp. 1201-1205
    • Morse, M.A.1    Califf, R.M.2    Sugarman, J.3
  • 10
    • 34447314711 scopus 로고    scopus 로고
    • Clinical trials bureaucracy: Unintended consequences of well-intentioned policy
    • Califf RM Clinical trials bureaucracy: Unintended consequences of well-intentioned policy. Clin Trials 2006; 3: 496-502.
    • (2006) Clin Trials , vol.3 , pp. 496-502
    • Califf, R.M.1
  • 11
    • 14744283495 scopus 로고    scopus 로고
    • A unified web-based query and notification system (QNS) for subject management, adverse events, regulatory, and IRB components of clinical trials
    • Mitchell R., Shah M., Ahmad S. et al. A unified web-based query and notification system (QNS) for subject management, adverse events, regulatory, and IRB components of clinical trials. Clin Trials 2005; 2: 61-71.
    • (2005) Clin Trials , vol.2 , pp. 61-71
    • Mitchell, R.1    Shah, M.2    Ahmad, S.3
  • 13
    • 56049120678 scopus 로고    scopus 로고
    • Available at: (accessed 16 January 2008)
    • caBIG® Community Website. Available at: https://cabig.nci.nih.gov/ (accessed 16 January 2008).
    • CaBIG® Community Website


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.