Evaluating the science and ethics of research on humans : a guide for IRB members / Dennis J. Mazur.
By: Mazur, Dennis John.
Baltimore : Johns Hopkins University Press, 2007Description: xi, 252 p. ; 23 cm.ISBN: 9780801885013 (hardcover : alk. paper); 9780801885020 (pbk. : alk. paper).Subject(s): Human experimentation in medicine -- Moral and ethical aspects | Medical ethics | Medicine -- Research -- Moral and ethical aspects | Ethics Committees, Research -- organization & administration -- United States | Human Experimentation -- ethics -- United States | Ethical Review -- United States | Human Experimentation -- standards -- United StatesGenre/Form: Print books.DDC classification: 174.2/8| Current location | Call number | Status | Date due | Barcode | Item holds |
|---|---|---|---|---|---|
| On Shelf | R853.H8 M39 2007 (Browse shelf) | Available | AU0000000005521 |
Browsing Alfaisal University Shelves , Shelving location: On Shelf Close shelf browser
|
|
|
|
|
|
|
||
| R853.H8 .H863 2014 Human subjects research regulation : perspectives on the future / | R853.H8 J66 1993 Bad blood : the Tuskegee syphilis experiment / | R853.H8 L54 2017 The Nazi doctors : medical killing and the psychology of genocide / | R853.H8 M39 2007 Evaluating the science and ethics of research on humans : a guide for IRB members / | R853.H8 R635 2004 Stiff : the curious lives of human cadavers / | R853.H8 S346 2015 The censor's hand : the misregulation of human-subject research / | R853.H8 W37 2006 Medical apartheid : the dark history of medical experimentation on Black Americans from colonial times to the present / |
Includes bibliographical references (p. 239-245) and index.
The IRB : its work, and its challenges -- What is an IRB, and what does it do? -- Basic terms and concepts used in IRB work -- What is risk? -- The scientific protocol and the informed consent form -- Prescreening of proposals -- The scientific protocol -- The informed consent form -- Recruitment, selection, and compensation of study participants -- Research involving questionnaires and surveys -- Protection of participants' privacy in research data and specimens -- The continuing work of the IRB -- The ethical issues of informed consent -- Continuing review, communication, and feedback -- Where are IRBs making mistakes, and how can we minimize mistakes? -- Strategies for managing the IRB workload and supporting IRB decision making -- Decision-making capacity and accountability in research.