Responsible research :: a systems approach to protecting research participants /
Issues addressed in the book include the need to distinguish the science, ethics, and conflict of interest reviews; desired qualifications for investigators and reviewers; the process of informed consent; federal, and institutional, oversight; and the role of accreditation. Recommendations for areas...
Gespeichert in:
Körperschaft: | |
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Weitere Verfasser: | , , |
Format: | Elektronisch E-Book |
Sprache: | English |
Veröffentlicht: |
Washington, D.C. :
National Academies Press,
©2003.
|
Schlagworte: | |
Online-Zugang: | Volltext |
Zusammenfassung: | Issues addressed in the book include the need to distinguish the science, ethics, and conflict of interest reviews; desired qualifications for investigators and reviewers; the process of informed consent; federal, and institutional, oversight; and the role of accreditation. Recommendations for areas of key interest include suggestions for legislative approaches, compensation for research-related injury, and the refocusing of institutional review boards. Responsible Research will be important to anyone interested in the issues that are relevant to the practice of using human subjects as research participants, but especially so to policy makers, research administrators, investigators, and research sponsors--but also including volunteers who may agree to serve as research participants. |
Beschreibung: | 1 online resource (xix, 290 pages) : illustrations |
Format: | Master and use copy. Digital master created according to Benchmark for Faithful Digital Reproductions of Monographs and Serials, Version 1. Digital Library Federation, December 2002. |
Bibliographie: | Includes bibliographical references and index. |
ISBN: | 030950046X 9780309500463 9786610209392 6610209391 1280209399 9781280209390 |
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049 | |a MAIN | ||
245 | 0 | 0 | |a Responsible research : |b a systems approach to protecting research participants / |c Daniel D. Federman, Kathi E. Hanna, and Laura Lyman Rodriguez, editors ; Committee on Assessing the System for Protecting Human Research Participants. |
260 | |a Washington, D.C. : |b National Academies Press, |c ©2003. | ||
300 | |a 1 online resource (xix, 290 pages) : |b illustrations | ||
336 | |a text |b txt |2 rdacontent | ||
337 | |a computer |b c |2 rdamedia | ||
338 | |a online resource |b cr |2 rdacarrier | ||
347 | |a data file | ||
504 | |a Includes bibliographical references and index. | ||
505 | 0 | |a 1. Introduction -- 2. A Systematic approach to human research participant protection programs -- 3. Back to basics: scientific, conflict of interest, and ethical review of research protocols -- 4. The Participant-investigator interface -- 5. Improving protection through oversight and data and safety monitoring -- 6. Improving human research participant protection program performance and clarifying roles -- 7. Improving an evolving national human research participant protection system. | |
588 | 0 | |a Print version record. | |
506 | |3 Use copy |f Restrictions unspecified |2 star |5 MiAaHDL | ||
533 | |a Electronic reproduction. |b [Place of publication not identified] : |c HathiTrust Digital Library, |d 2010. |5 MiAaHDL | ||
538 | |a Master and use copy. Digital master created according to Benchmark for Faithful Digital Reproductions of Monographs and Serials, Version 1. Digital Library Federation, December 2002. |u http://purl.oclc.org/DLF/benchrepro0212 |5 MiAaHDL | ||
583 | 1 | |a digitized |c 2010 |h HathiTrust Digital Library |l committed to preserve |2 pda |5 MiAaHDL | |
520 | 8 | |a Issues addressed in the book include the need to distinguish the science, ethics, and conflict of interest reviews; desired qualifications for investigators and reviewers; the process of informed consent; federal, and institutional, oversight; and the role of accreditation. Recommendations for areas of key interest include suggestions for legislative approaches, compensation for research-related injury, and the refocusing of institutional review boards. Responsible Research will be important to anyone interested in the issues that are relevant to the practice of using human subjects as research participants, but especially so to policy makers, research administrators, investigators, and research sponsors--but also including volunteers who may agree to serve as research participants. | |
546 | |a English. | ||
650 | 0 | |a Human experimentation in medicine |x Moral and ethical aspects. | |
650 | 0 | |a Medical ethics. |0 http://id.loc.gov/authorities/subjects/sh85082929 | |
650 | 0 | |a Medical protocols. |0 http://id.loc.gov/authorities/subjects/sh85083005 | |
650 | 0 | |a Patients |x Legal status, laws, etc. |0 http://id.loc.gov/authorities/subjects/sh88006248 | |
650 | 0 | |a Human experimentation in medicine. |0 http://id.loc.gov/authorities/subjects/sh85062870 | |
650 | 0 | |a Institutional review boards (Medicine) |0 http://id.loc.gov/authorities/subjects/sh2001010894 | |
650 | 0 | |a Informed consent (Medical law) |0 http://id.loc.gov/authorities/subjects/sh85066306 | |
650 | 1 | |a Safety. | |
650 | 2 | |a Clinical Protocols | |
650 | 2 | |a Human Experimentation | |
650 | 2 | |a Patient Rights | |
650 | 2 | |a Safety | |
650 | 2 | |a Ethics, Medical |0 https://id.nlm.nih.gov/mesh/D004992 | |
650 | 2 | |a Truth Disclosure |0 https://id.nlm.nih.gov/mesh/D014342 | |
650 | 2 | 2 | |a Clinical Trials Data Monitoring Committees |
650 | 2 | 2 | |a Conflict of Interest |
650 | 2 | 2 | |a Ethical Review |
650 | 2 | 2 | |a Ethics Committees, Research |
650 | 2 | 2 | |a Government Regulation |
650 | 2 | 2 | |a Human Experimentation |x standards |
650 | 2 | 2 | |a Informed Consent |
650 | 2 | 2 | |a Public Policy |
650 | 2 | 2 | |a Research Subjects |
650 | 2 | 2 | |a Researcher-Subject Relations |
651 | 2 | |a United States | |
650 | 6 | |a Expérimentation humaine en médecine |x Aspect moral. | |
650 | 6 | |a Éthique médicale. | |
650 | 6 | |a Protocoles médicaux. | |
650 | 6 | |a Expérimentation humaine en médecine. | |
650 | 6 | |a Comités d'éthique de la recherche. | |
650 | 6 | |a Consentement éclairé (Droit médical) | |
650 | 7 | |a MEDICAL |x Ethics. |2 bisacsh | |
650 | 7 | |a Human experimentation in medicine |x Moral and ethical aspects |2 fast | |
650 | 7 | |a Medical ethics |2 fast | |
650 | 7 | |a Medical protocols |2 fast | |
650 | 7 | |a Patients |x Legal status, laws, etc. |2 fast | |
650 | 1 | 7 | |a Onderzoek. |2 gtt |
650 | 1 | 7 | |a Medische ethiek. |2 gtt |
650 | 1 | 7 | |a Patiëntenrecht. |2 gtt |
655 | 7 | |a Juvenile works |2 fast | |
700 | 1 | |a Federman, Daniel D., |d 1928-2017. |1 https://id.oclc.org/worldcat/entity/E39PBJkMPwXhbPJ8VYVbg46HYP | |
700 | 1 | |a Hanna, Kathi E. |0 http://id.loc.gov/authorities/names/n89222901 | |
700 | 1 | |a Rodriguez, Laura Lyman. |0 http://id.loc.gov/authorities/names/n2002136048 | |
710 | 2 | |a Institute of Medicine (U.S.). |b Committee on Assessing the System for Protecting Human Research Participants. |0 http://id.loc.gov/authorities/names/n2002136049 | |
758 | |i has work: |a Responsible research (Text) |1 https://id.oclc.org/worldcat/entity/E39PCFFKjm7fR6QpPPC3MxQH4q |4 https://id.oclc.org/worldcat/ontology/hasWork | ||
776 | 0 | 8 | |i Print version: |t Responsible research. |d Washington, D.C. : National Academies Press, ©2003 |z 0309084881 |w (DLC) 2002015090 |w (OCoLC)50639306 |
856 | 4 | 0 | |l FWS01 |p ZDB-4-EBA |q FWS_PDA_EBA |u https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=87116 |3 Volltext |
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Datensatz im Suchindex
DE-BY-FWS_katkey | ZDB-4-EBA-ocm52817279 |
---|---|
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adam_text | |
any_adam_object | |
author2 | Federman, Daniel D., 1928-2017 Hanna, Kathi E. Rodriguez, Laura Lyman |
author2_role | |
author2_variant | d d f dd ddf k e h ke keh l l r ll llr |
author_GND | http://id.loc.gov/authorities/names/n89222901 http://id.loc.gov/authorities/names/n2002136048 |
author_corporate | Institute of Medicine (U.S.). Committee on Assessing the System for Protecting Human Research Participants |
author_corporate_role | |
author_facet | Federman, Daniel D., 1928-2017 Hanna, Kathi E. Rodriguez, Laura Lyman Institute of Medicine (U.S.). Committee on Assessing the System for Protecting Human Research Participants |
author_sort | Federman, Daniel D., 1928-2017 |
building | Verbundindex |
bvnumber | localFWS |
callnumber-first | R - Medicine |
callnumber-label | R853 |
callnumber-raw | R853.H8 R476 2003eb |
callnumber-search | R853.H8 R476 2003eb |
callnumber-sort | R 3853 H8 R476 42003EB |
callnumber-subject | R - General Medicine |
collection | ZDB-4-EBA |
contents | 1. Introduction -- 2. A Systematic approach to human research participant protection programs -- 3. Back to basics: scientific, conflict of interest, and ethical review of research protocols -- 4. The Participant-investigator interface -- 5. Improving protection through oversight and data and safety monitoring -- 6. Improving human research participant protection program performance and clarifying roles -- 7. Improving an evolving national human research participant protection system. |
ctrlnum | (OCoLC)52817279 |
dewey-full | 174/.28 |
dewey-hundreds | 100 - Philosophy & psychology |
dewey-ones | 174 - Occupational ethics |
dewey-raw | 174/.28 |
dewey-search | 174/.28 |
dewey-sort | 3174 228 |
dewey-tens | 170 - Ethics (Moral philosophy) |
discipline | Philosophie |
format | Electronic eBook |
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Federman, Kathi E. Hanna, and Laura Lyman Rodriguez, editors ; Committee on Assessing the System for Protecting Human Research Participants.</subfield></datafield><datafield tag="260" ind1=" " ind2=" "><subfield code="a">Washington, D.C. :</subfield><subfield code="b">National Academies Press,</subfield><subfield code="c">©2003.</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 online resource (xix, 290 pages) :</subfield><subfield code="b">illustrations</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">computer</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">online resource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="347" ind1=" " ind2=" "><subfield code="a">data file</subfield></datafield><datafield tag="504" ind1=" " ind2=" "><subfield code="a">Includes bibliographical references and index.</subfield></datafield><datafield tag="505" ind1="0" ind2=" "><subfield code="a">1. Introduction -- 2. A Systematic approach to human research participant protection programs -- 3. Back to basics: scientific, conflict of interest, and ethical review of research protocols -- 4. The Participant-investigator interface -- 5. Improving protection through oversight and data and safety monitoring -- 6. Improving human research participant protection program performance and clarifying roles -- 7. Improving an evolving national human research participant protection system.</subfield></datafield><datafield tag="588" ind1="0" ind2=" "><subfield code="a">Print version record.</subfield></datafield><datafield tag="506" ind1=" " ind2=" "><subfield code="3">Use copy</subfield><subfield code="f">Restrictions unspecified</subfield><subfield code="2">star</subfield><subfield code="5">MiAaHDL</subfield></datafield><datafield tag="533" ind1=" " ind2=" "><subfield code="a">Electronic reproduction.</subfield><subfield code="b">[Place of publication not identified] :</subfield><subfield code="c">HathiTrust Digital Library,</subfield><subfield code="d">2010.</subfield><subfield code="5">MiAaHDL</subfield></datafield><datafield tag="538" ind1=" " ind2=" "><subfield code="a">Master and use copy. Digital master created according to Benchmark for Faithful Digital Reproductions of Monographs and Serials, Version 1. Digital Library Federation, December 2002.</subfield><subfield code="u">http://purl.oclc.org/DLF/benchrepro0212</subfield><subfield code="5">MiAaHDL</subfield></datafield><datafield tag="583" ind1="1" ind2=" "><subfield code="a">digitized</subfield><subfield code="c">2010</subfield><subfield code="h">HathiTrust Digital Library</subfield><subfield code="l">committed to preserve</subfield><subfield code="2">pda</subfield><subfield code="5">MiAaHDL</subfield></datafield><datafield tag="520" ind1="8" ind2=" "><subfield code="a">Issues addressed in the book include the need to distinguish the science, ethics, and conflict of interest reviews; desired qualifications for investigators and reviewers; the process of informed consent; federal, and institutional, oversight; and the role of accreditation. Recommendations for areas of key interest include suggestions for legislative approaches, compensation for research-related injury, and the refocusing of institutional review boards. Responsible Research will be important to anyone interested in the issues that are relevant to the practice of using human subjects as research participants, but especially so to policy makers, research administrators, investigators, and research sponsors--but also including volunteers who may agree to serve as research participants.</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">English.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Human experimentation in medicine</subfield><subfield code="x">Moral and ethical aspects.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Medical ethics.</subfield><subfield code="0">http://id.loc.gov/authorities/subjects/sh85082929</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Medical protocols.</subfield><subfield code="0">http://id.loc.gov/authorities/subjects/sh85083005</subfield></datafield><datafield tag="650" ind1=" " 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genre | Juvenile works fast |
genre_facet | Juvenile works |
geographic | United States |
geographic_facet | United States |
id | ZDB-4-EBA-ocm52817279 |
illustrated | Illustrated |
indexdate | 2024-11-27T13:15:27Z |
institution | BVB |
institution_GND | http://id.loc.gov/authorities/names/n2002136049 |
isbn | 030950046X 9780309500463 9786610209392 6610209391 1280209399 9781280209390 |
language | English |
oclc_num | 52817279 |
open_access_boolean | |
owner | MAIN DE-863 DE-BY-FWS |
owner_facet | MAIN DE-863 DE-BY-FWS |
physical | 1 online resource (xix, 290 pages) : illustrations |
psigel | ZDB-4-EBA |
publishDate | 2003 |
publishDateSearch | 2003 |
publishDateSort | 2003 |
publisher | National Academies Press, |
record_format | marc |
spelling | Responsible research : a systems approach to protecting research participants / Daniel D. Federman, Kathi E. Hanna, and Laura Lyman Rodriguez, editors ; Committee on Assessing the System for Protecting Human Research Participants. Washington, D.C. : National Academies Press, ©2003. 1 online resource (xix, 290 pages) : illustrations text txt rdacontent computer c rdamedia online resource cr rdacarrier data file Includes bibliographical references and index. 1. Introduction -- 2. A Systematic approach to human research participant protection programs -- 3. Back to basics: scientific, conflict of interest, and ethical review of research protocols -- 4. The Participant-investigator interface -- 5. Improving protection through oversight and data and safety monitoring -- 6. Improving human research participant protection program performance and clarifying roles -- 7. Improving an evolving national human research participant protection system. Print version record. Use copy Restrictions unspecified star MiAaHDL Electronic reproduction. [Place of publication not identified] : HathiTrust Digital Library, 2010. MiAaHDL Master and use copy. Digital master created according to Benchmark for Faithful Digital Reproductions of Monographs and Serials, Version 1. Digital Library Federation, December 2002. http://purl.oclc.org/DLF/benchrepro0212 MiAaHDL digitized 2010 HathiTrust Digital Library committed to preserve pda MiAaHDL Issues addressed in the book include the need to distinguish the science, ethics, and conflict of interest reviews; desired qualifications for investigators and reviewers; the process of informed consent; federal, and institutional, oversight; and the role of accreditation. Recommendations for areas of key interest include suggestions for legislative approaches, compensation for research-related injury, and the refocusing of institutional review boards. Responsible Research will be important to anyone interested in the issues that are relevant to the practice of using human subjects as research participants, but especially so to policy makers, research administrators, investigators, and research sponsors--but also including volunteers who may agree to serve as research participants. English. Human experimentation in medicine Moral and ethical aspects. Medical ethics. http://id.loc.gov/authorities/subjects/sh85082929 Medical protocols. http://id.loc.gov/authorities/subjects/sh85083005 Patients Legal status, laws, etc. http://id.loc.gov/authorities/subjects/sh88006248 Human experimentation in medicine. http://id.loc.gov/authorities/subjects/sh85062870 Institutional review boards (Medicine) http://id.loc.gov/authorities/subjects/sh2001010894 Informed consent (Medical law) http://id.loc.gov/authorities/subjects/sh85066306 Safety. Clinical Protocols Human Experimentation Patient Rights Safety Ethics, Medical https://id.nlm.nih.gov/mesh/D004992 Truth Disclosure https://id.nlm.nih.gov/mesh/D014342 Clinical Trials Data Monitoring Committees Conflict of Interest Ethical Review Ethics Committees, Research Government Regulation Human Experimentation standards Informed Consent Public Policy Research Subjects Researcher-Subject Relations United States Expérimentation humaine en médecine Aspect moral. Éthique médicale. Protocoles médicaux. Expérimentation humaine en médecine. Comités d'éthique de la recherche. Consentement éclairé (Droit médical) MEDICAL Ethics. bisacsh Human experimentation in medicine Moral and ethical aspects fast Medical ethics fast Medical protocols fast Patients Legal status, laws, etc. fast Onderzoek. gtt Medische ethiek. gtt Patiëntenrecht. gtt Juvenile works fast Federman, Daniel D., 1928-2017. https://id.oclc.org/worldcat/entity/E39PBJkMPwXhbPJ8VYVbg46HYP Hanna, Kathi E. http://id.loc.gov/authorities/names/n89222901 Rodriguez, Laura Lyman. http://id.loc.gov/authorities/names/n2002136048 Institute of Medicine (U.S.). Committee on Assessing the System for Protecting Human Research Participants. http://id.loc.gov/authorities/names/n2002136049 has work: Responsible research (Text) https://id.oclc.org/worldcat/entity/E39PCFFKjm7fR6QpPPC3MxQH4q https://id.oclc.org/worldcat/ontology/hasWork Print version: Responsible research. Washington, D.C. : National Academies Press, ©2003 0309084881 (DLC) 2002015090 (OCoLC)50639306 FWS01 ZDB-4-EBA FWS_PDA_EBA https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=87116 Volltext |
spellingShingle | Responsible research : a systems approach to protecting research participants / 1. Introduction -- 2. A Systematic approach to human research participant protection programs -- 3. Back to basics: scientific, conflict of interest, and ethical review of research protocols -- 4. The Participant-investigator interface -- 5. Improving protection through oversight and data and safety monitoring -- 6. Improving human research participant protection program performance and clarifying roles -- 7. Improving an evolving national human research participant protection system. Human experimentation in medicine Moral and ethical aspects. Medical ethics. http://id.loc.gov/authorities/subjects/sh85082929 Medical protocols. http://id.loc.gov/authorities/subjects/sh85083005 Patients Legal status, laws, etc. http://id.loc.gov/authorities/subjects/sh88006248 Human experimentation in medicine. http://id.loc.gov/authorities/subjects/sh85062870 Institutional review boards (Medicine) http://id.loc.gov/authorities/subjects/sh2001010894 Informed consent (Medical law) http://id.loc.gov/authorities/subjects/sh85066306 Safety. Clinical Protocols Human Experimentation Patient Rights Safety Ethics, Medical https://id.nlm.nih.gov/mesh/D004992 Truth Disclosure https://id.nlm.nih.gov/mesh/D014342 Clinical Trials Data Monitoring Committees Conflict of Interest Ethical Review Ethics Committees, Research Government Regulation Human Experimentation standards Informed Consent Public Policy Research Subjects Researcher-Subject Relations Expérimentation humaine en médecine Aspect moral. Éthique médicale. Protocoles médicaux. Expérimentation humaine en médecine. Comités d'éthique de la recherche. Consentement éclairé (Droit médical) MEDICAL Ethics. bisacsh Human experimentation in medicine Moral and ethical aspects fast Medical ethics fast Medical protocols fast Patients Legal status, laws, etc. fast Onderzoek. gtt Medische ethiek. gtt Patiëntenrecht. gtt |
subject_GND | http://id.loc.gov/authorities/subjects/sh85082929 http://id.loc.gov/authorities/subjects/sh85083005 http://id.loc.gov/authorities/subjects/sh88006248 http://id.loc.gov/authorities/subjects/sh85062870 http://id.loc.gov/authorities/subjects/sh2001010894 http://id.loc.gov/authorities/subjects/sh85066306 https://id.nlm.nih.gov/mesh/D004992 https://id.nlm.nih.gov/mesh/D014342 |
title | Responsible research : a systems approach to protecting research participants / |
title_auth | Responsible research : a systems approach to protecting research participants / |
title_exact_search | Responsible research : a systems approach to protecting research participants / |
title_full | Responsible research : a systems approach to protecting research participants / Daniel D. Federman, Kathi E. Hanna, and Laura Lyman Rodriguez, editors ; Committee on Assessing the System for Protecting Human Research Participants. |
title_fullStr | Responsible research : a systems approach to protecting research participants / Daniel D. Federman, Kathi E. Hanna, and Laura Lyman Rodriguez, editors ; Committee on Assessing the System for Protecting Human Research Participants. |
title_full_unstemmed | Responsible research : a systems approach to protecting research participants / Daniel D. Federman, Kathi E. Hanna, and Laura Lyman Rodriguez, editors ; Committee on Assessing the System for Protecting Human Research Participants. |
title_short | Responsible research : |
title_sort | responsible research a systems approach to protecting research participants |
title_sub | a systems approach to protecting research participants / |
topic | Human experimentation in medicine Moral and ethical aspects. Medical ethics. http://id.loc.gov/authorities/subjects/sh85082929 Medical protocols. http://id.loc.gov/authorities/subjects/sh85083005 Patients Legal status, laws, etc. http://id.loc.gov/authorities/subjects/sh88006248 Human experimentation in medicine. http://id.loc.gov/authorities/subjects/sh85062870 Institutional review boards (Medicine) http://id.loc.gov/authorities/subjects/sh2001010894 Informed consent (Medical law) http://id.loc.gov/authorities/subjects/sh85066306 Safety. Clinical Protocols Human Experimentation Patient Rights Safety Ethics, Medical https://id.nlm.nih.gov/mesh/D004992 Truth Disclosure https://id.nlm.nih.gov/mesh/D014342 Clinical Trials Data Monitoring Committees Conflict of Interest Ethical Review Ethics Committees, Research Government Regulation Human Experimentation standards Informed Consent Public Policy Research Subjects Researcher-Subject Relations Expérimentation humaine en médecine Aspect moral. Éthique médicale. Protocoles médicaux. Expérimentation humaine en médecine. Comités d'éthique de la recherche. Consentement éclairé (Droit médical) MEDICAL Ethics. bisacsh Human experimentation in medicine Moral and ethical aspects fast Medical ethics fast Medical protocols fast Patients Legal status, laws, etc. fast Onderzoek. gtt Medische ethiek. gtt Patiëntenrecht. gtt |
topic_facet | Human experimentation in medicine Moral and ethical aspects. Medical ethics. Medical protocols. Patients Legal status, laws, etc. Human experimentation in medicine. Institutional review boards (Medicine) Informed consent (Medical law) Safety. Clinical Protocols Human Experimentation Patient Rights Safety Ethics, Medical Truth Disclosure Clinical Trials Data Monitoring Committees Conflict of Interest Ethical Review Ethics Committees, Research Government Regulation Human Experimentation standards Informed Consent Public Policy Research Subjects Researcher-Subject Relations United States Expérimentation humaine en médecine Aspect moral. Éthique médicale. Protocoles médicaux. Expérimentation humaine en médecine. Comités d'éthique de la recherche. Consentement éclairé (Droit médical) MEDICAL Ethics. Human experimentation in medicine Moral and ethical aspects Medical ethics Medical protocols Onderzoek. Medische ethiek. Patiëntenrecht. Juvenile works |
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