Protecting research subjects--the crisis at Johns Hopkins.
about
A CTSA-sponsored program for clinical research coordination: networking, education, and mentoringEvaluation of a self-paced learning module to teach responsible literature searching for researchAcademic health sciences library research support.The new research ethic: will oversight requirements sink forensic research?Information-seeking behavior and use of information resources by clinical research coordinatorsVariations among Institutional Review Board reviews in a multisite health services research study.The research subject advocate at minority Clinical Research Centers: an added resource for protection of human subjects.Safety of and cellular response to segmental bronchoprovocation in allergic asthmaRegulating research with human subjects--is the system broken?Streamlining the clinical research enterprise.Misconduct in medical research: whose responsibility?Supporting whistleblowers in academic medicine: training and respecting the courage of professional conscience.Key concepts of clinical trials: a narrative reviewEthics review procedures for research in developing countries: a basic presumption of guiltThe complexities of individual financial conflicts of interest.Caveat lector.Investigative bronchoprovocation and bronchoscopy in airway diseasesLimits on risks for healthy volunteers in biomedical research.Administrative and research policies required to bring cellular therapies from the research laboratory to the patient's bedside.The reporting of IRB review in journal articles presenting HIV research conducted in the developing worldMedical research in children: ethical issues.Paternalism and utilitarianism in research with human participants.Policy needs regarding the duty to protect in epidemiological research with high-risk populations.First-in-human trial participants: not a vulnerable population, but vulnerable nonetheless.The impact of minor adverse event tracking on subject safety: a web-based system.Strategies to minimize risks and exploitation in phase one trials on healthy subjects.Failsafe automation of Phase II clinical trial interim monitoring for stopping rules.IRB decision-making with imperfect knowledge: a framework for evidence-based research ethics review.Assessing the quality of human research protection programs to improve protection of human subjects participating in clinical trials.An Assessment of the Human Subjects Protection Review Process for Exempt Research.Getting it right: industry sponsorship and medical research.Controlled human malaria infection trials: How tandems of trust and control construct scientific knowledge.Regional ethics organizations for protection of human research participants.Author response to letter regarding "Children in clinical research: a conflict of moral values" (AJOB 3:1).Paying Research Participants: Regulatory Uncertainty, Conceptual Confusion, and a Path Forward.Social movements in health: an introduction.Empty ethics: the problem with informed consent.Serial Participation and the Ethics of Phase 1 Healthy Volunteer Research.Where are the institutional review boards?The limitations of "vulnerability" as a protection for human research participants.
P2860
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P2860
Protecting research subjects--the crisis at Johns Hopkins.
description
2002 nî lūn-bûn
@nan
2002年の論文
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2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Protecting research subjects--the crisis at Johns Hopkins.
@en
Protecting research subjects--the crisis at Johns Hopkins.
@nl
type
label
Protecting research subjects--the crisis at Johns Hopkins.
@en
Protecting research subjects--the crisis at Johns Hopkins.
@nl
prefLabel
Protecting research subjects--the crisis at Johns Hopkins.
@en
Protecting research subjects--the crisis at Johns Hopkins.
@nl
P1476
Protecting research subjects--the crisis at Johns Hopkins.
@en
P304
P356
10.1056/NEJM200202283460924
P407
P577
2002-02-01T00:00:00Z