Responsible research : a systems approach to protecting research participants /

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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...

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Détails bibliographiques
Cote:Libro Electrónico
Collectivité auteur: Institute of Medicine (U.S.). Committee on Assessing the System for Protecting Human Research Participants
Autres auteurs: Federman, Daniel D., 1928-2017, Hanna, Kathi E., Rodriguez, Laura Lyman
Format: Électronique eBook
Langue:Inglés
Publié: Washington, D.C. : National Academies Press, ©2003.
Sujets:
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
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.
United States
Juvenile works
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