Protecting Study Volunteers in Research: A Manual for Investigative Sites. Dieser Artikel ist nicht verfügbar.
McGuire-Dunn, Cynthia, M.D.,Chadwick, Gary L.
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Sprache: Englisch
Verlag: CenterWatch, 2004
- Softcover
- Gebraucht
Anbieter: HPB-Diamond, Dallas, TX, USAHPB-Diamond
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Softcover
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- Titel
- Protecting Study Volunteers in Research: A Manual for Investigative Sites
- Autor
- McGuire-Dunn, Cynthia, M.D.,Chadwick, Gary L.
- Verlag
- CenterWatch
- Erscheinungsjahr
- 2004
- Zustand
- Very Good
- Einband
- paperback
- Sprache
- Englisch
- ISBN-10
- 1930624441
- ISBN-13
- 9781930624443
- Auflage
- 3. Auflage
This well-organized and concise manual teaches organizations how to successfully implement the highest standards of safe and ethical treatment of study volunteers while addressing current and emerging issues that are critical to our system of human subject protection oversight.
Protecting Study Volunteers in Research is a suggested educational resource by NIH and FDA (source: NIH Notice OD-00-039, 2000, page 37841, Federal Registry 2002) and has become required reading in many academic institutions, IRBs, investigative sites, and for many Biopharmaceutical and CRO companies.
Written by Cynthia Dunn, M.D. of Western Institutional Review Board and Gary Chadwick, Pharm.D., M.P.H. of the University of Rochester, this manual has been developed in accordance with ACCME. Readers can apply for CME credits or nursing contact hours. An exam is provided with each manual and is also available online.
Topics covered include:
*Conflicts of interest in research
*Participant recruitment and retention in clinical trials
*Research with secondary subjects, tissue studies, and records review
*Historical perspectives on human subject research
*Updated ethics and federal regulations
*Roles and responsibilities of institutions and independent sites
*Roles and responsibilities of investigators and the study process
Protecting Study Volunteers in Research is a suggested educational resource by NIH and FDA (source: NIH Notice OD-00-039, 2000, page 37841, Federal Registry 2002) and has become required reading in many academic institutions, IRBs, investigative sites, and for many Biopharmaceutical and CRO companies.
Written by Cynthia Dunn, M.D. of Western Institutional Review Board and Gary Chadwick, Pharm.D., M.P.H. of the University of Rochester, this manual has been developed in accordance with ACCME. Readers can apply for CME credits or nursing contact hours. An exam is provided with each manual and is also available online.
Topics covered include:
*Conflicts of interest in research
*Participant recruitment and retention in clinical trials
*Research with secondary subjects, tissue studies, and records review
*Historical perspectives on human subject research
*Updated ethics and federal regulations
*Roles and responsibilities of institutions and independent sites
*Roles and responsibilities of investigators and the study process
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