Data Sharing in Historical PerspectiveSharing Research Data to Improve Public Health: A Funder PerspectiveBest Practices for Ethical Sharing of Individual-Level Health Research Data From Low- and Middle-Income SettingsViews of Ethical Best Practices in Sharing Individual-Level Data From Medical and Public Health Research: A Systematic Scoping ReviewThe vulnerabilities of orphaned children participating in research: a critical review and factors for consideration for participation in biomedical and behavioral researchResearch ethics education for community-engaged research: a review and research agendaThe MICHR Genomic DNA BioLibrary: An Empirical Study of the Ethics of Biorepository DevelopmentThe views of quality improvement professionals and comparative effectiveness researchers on ethics, IRBs, and oversightCapacity building from the inside out: development and evaluation of a CITI ethics certification training module for American Indian and Alaska Native community researchersViews of academic and community partners regarding participant protections and research integrity: a pilot focus group studyTrust, Respect, and Reciprocity: Informing Culturally Appropriate Data-Sharing Practice in VietnamConsent and community engagement in diverse research contextsInvestigator Experiences and Attitudes About Research With BiospecimensInvolving Research Stakeholders in Developing Policy on Sharing Public Health Research Data in Kenya: Views on Fair Process for Informed Consent, Access Oversight, and Community Engagement.Addressing Global Data Sharing ChallengesDeveloping Ethical Practices for Public Health Research Data Sharing in South Africa: The Views and Experiences From a Diverse Sample of Research StakeholdersData Rights and Responsibilities: A Human Rights Perspective on Data SharingThe INDEPTH Data Repository: An International Resource for Longitudinal Population and Health Data From Health and Demographic Surveillance SystemsSweat, Skepticism, and Uncharted Territory: A Qualitative Study of Opinions on Data Sharing Among Public Health Researchers and Research Participants in Mumbai, IndiaPerceived Benefits, Harms, and Views About How to Share Data Responsibly: A Qualitative Study of Experiences With and Attitudes Toward Data Sharing Among Research Staff and Community Representatives in ThailandSharing Public Health Research Data: Toward the Development of Ethical Data-Sharing Practice in Low- and Middle-Income SettingsAttitudes toward genetic research review: results from a national survey of professionals involved in human subjects protectionA Reflection on a Data Curation JourneySelf-Consent for HIV Prevention Research Involving Sexual and Gender Minority Youth: Reducing Barriers Through Evidence-Based EthicsAre Research Ethics Committees Prepared for Community-Based Participatory Research?Community-based participatory research in disaster preparedness among linguistically isolated populations: a public health perspective.Enhancing HIV vaccine trial consent preparedness among street drug usersToward ethical research practice with deaf participants.Evaluating international collaboration: differential perceptions of partnership in a CBPR project in Ghana.Social and structural constraints on disclosure and informed consent for HIV survey research involving female sex workers and their bar managers in the Philippines.A collaborative methodology for investigating the ethical conduct of research on female sex workers in the Philippines.Applying research ethics guidelines: the view from a sub-saharan research ethics committee.Privacy and confidentiality resources.Misbehaviors of front-line research personnel and the integrity of community-based researchSham surgery trial controls: perspectives of patients and their relatives.Local IRBs vs. federal agencies: shifting dynamics, systems, and relationships.An analysis of online courses in research ethics in the Fogarty-sponsored bioethics training programs.I'm positive, but i'm negative: Competing Voices in Informed Consent and Implications for HIV vaccine trials.A New Measure of Research Participant Burden: Brief ReportCritical illness research involving collection of genomic data: the conundrum posed by low levels of genomic literacy among surrogate decision makers for critically ill patients.
P1433
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P1433
description
journal
@en
periodiek van uitgeverij SAGE Publications
@nl
مجلة
@ar
name
Journal of Empirical Research on Human Research Ethics
@en
type
label
Journal of Empirical Research on Human Research Ethics
@en
prefLabel
Journal of Empirical Research on Human Research Ethics
@en
P243
P3181
P1055
P1058
P1156
17800156703
P123
P1230
jempreshumreseth
P1277
P1476
Journal of Empirical Research on Human Research Ethics
@en
P236
P243
P31
P3181
P407
P571
2006-01-01T00:00:00Z