Reforming the regulations governing research with human subjects.
about
Fostering IRB collaboration for review of international researchInstitutional Review Boards: Purpose and ChallengesThe wave has finally broken: now what?Local IRBs vs. federal agencies: shifting dynamics, systems, and relationships.Recommendations for ethical approaches to genotype-driven research recruitment.Is it ethical to prevent secondary use of stored biological samples and data derived from consenting research participants? The case of Malawi.Role for CTSAs in leveraging a distributed research infrastructure to engage diverse stakeholders in emergent research policy developmentMaking general internal medicine research relevant to the older patient with multiple chronic comorbidities.Public preferences about secondary uses of electronic health information.What research ethics should learn from genomics and society research: lessons from the ELSI Congress of 2011.A national strategy to develop pragmatic clinical trials infrastructure.What makes public health studies ethical? Dissolving the boundary between research and practiceThe ethics police?: IRBs' views concerning their power.How variability in the institutional review board review process affects minimal-risk multisite health services research.From anonymity to "open doors": IRB responses to tensions with researchers.Participant informed consent in cluster randomized trials: review.Procedure versus process: ethical paradigms and the conduct of qualitative research.Observational research with adolescents: a framework for the management of the parental permissionImproving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trialsInformed consent for biobanking: consensus-based guidelines for adequate comprehension.Actors involved in the regulation of clinical research: comparison of Finland to England, Canada, and the USA.Risk assessment and management for medically complex potential living kidney donors: a few deontological criteria and ethical values.Variability in obtaining institutional review board approval for quality improvement activities in residency programs.Canada's new ethical guidelines for research with humans: a critique and comparison with the United States.The importance of purpose: moving beyond consent in the societal use of personal health information.Becoming partners, retaining autonomy: ethical considerations on the development of precision medicine.A pilot test of the new Swiss regulatory procedure for categorizing clinical trials by risk: A randomized controlled trial.Specimen collection for induced pluripotent stem cell research: harmonizing the approach to informed consentViews of IRBs Concerning their Local Ecologies: Perceptions of Relationships, Systems, and Tensions between IRBs and their Institutions.Implementation of timeline reforms speeds initiation of National Cancer Institute-sponsored trials.Characterizing biobank organizations in the U.S.: results from a national surveyEthics Review for a Multi-Site Project Involving Tribal Nations in the Northern Plains.How IRB leaders view and approach challenges raised by industry-funded research.Ethical and practical challenges to studying patients who opt out of large-scale biorepository research.Regulatory challenges associated with conducting multicountry clinical trials in resource-limited settings.Use of human specimens in research: the evolving United States regulatory, policy, and scientific landscape.Biobanks containing clinical specimens: defining characteristics, policies, and practices.Governance of clinical research.Revolution or reform in human subjects research oversight.The role of the institutional review board in the oversight of the ethical aspects of human studies research.
P2860
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P2860
Reforming the regulations governing research with human subjects.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh-hant
name
Reforming the regulations governing research with human subjects.
@en
Reforming the regulations governing research with human subjects.
@nl
type
label
Reforming the regulations governing research with human subjects.
@en
Reforming the regulations governing research with human subjects.
@nl
prefLabel
Reforming the regulations governing research with human subjects.
@en
Reforming the regulations governing research with human subjects.
@nl
P356
P1476
Reforming the regulations governing research with human subjects.
@en
P2093
Jerry Menikoff
P304
P356
10.1056/NEJMSB1106942
P407
P577
2011-07-25T00:00:00Z