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Casebook on ethical issues in international health research

서명/저자사항
Casebook on ethical issues in international health research
발행사항
Geneva, Switzerland : World Health Organization, 2009.
형태사항
209 p. : ill. ; 30 cm.
주기사항
This casebook has been developed as a teaching tool for instructors and workshop leaders rather than as a textbook for students or workshop participants. There is no need for participants to have copies of the casebook: facilitators can provide participants with individual case studies and chapter introductions relevant to the research ethics topic being addressed. Individual case studies and chapter introductions relevant to the research ethics topic being addressed can be photocopied from the print version or downloaded from the WHO web site without additional permission from WHO, unless the planned use is in conjunction with commercial purposes Suggested readings and resources: p. 193-207 I. Defining "research" -- II. Issues in study design . -- III. Harm and benefit -- IV. Voluntary informed consent -- V. Standard of care -- VI. Obligations to participants and communities -- VII. Privacy and confidentiality -- VIII. Professional ethics
소장정보
위치등록번호청구기호 / 출력상태반납예정일
이용 가능 (1)
자료실WM018280대출가능-
이용 가능 (1)
  • 등록번호
    WM018280
    상태/반납예정일
    대출가능
    -
    위치/청구기호(출력)
    자료실
책 소개
This casebook has been developed as a teaching tool for instructors and workshop leaders rather than as a textbook for students or workshop participants. There is no need for participants to have copies of the casebook: facilitators can provide participants with individual case studies and chapter introductions relevant to the research ethics topic being addressed. Individual case studies and chapter introductions relevant to the research ethics topic being addressed can be photocopied from the print version or downloaded from the WHO web site without additional permission from WHO, unless the planned use is in conjunction with commercial purposes.
목차
I. Defining "research" -- II. Issues in study design . -- III. Harm and benefit -- IV. Voluntary informed consent -- V. Standard of care -- VI. Obligations to participants and communities -- VII. Privacy and confidentiality -- VIII. Professional ethics
주제어