Issue Information

Ethical Issues Faced by Data Monitoring Committees: Results from an Exploratory Qualitative Study
von: Seema K. Shah, et al.
Veröffentlicht: (2024)

Perspectives of Information Access in the Informed Consent Process for Clinical Research Participation in Australia
von: Fleur O'Hare, et al.
Veröffentlicht: (2026)

Exception from Informed Consent in Emergency Care Research: Reports from a Workshop Addressing “Edge Cases”
von: Jeremy Brown, et al.
Veröffentlicht: (2025)

Expectations, Tensions, and Brokerage: A Discourse Analysis of Community Engagement with Health Research in South Africa
von: Sonja Klingberg, et al.
Veröffentlicht: (2025)

Navigating Challenges with IRB Review for Community‐Engaged Research with Transgender Youth in the United States
von: Alic G. Shook, et al.
Veröffentlicht: (2025)

Stakeholder Views on Novel Consent Forms for an Acute Stroke Trial
von: Candace D. Speight, et al.
Veröffentlicht: (2025)

Our Theater of Anonymity
von: Sara Meeder, et al.
Veröffentlicht: (2025)

What's in a Lie? How Researchers Judge the Justifiability of Deception
von: Kamiel Verbeke, et al.
Veröffentlicht: (2025)

Brain Organoid Research in a Post‐Dobbs World
von: Christine N. Coughlin, et al.
Veröffentlicht: (2025)

Engaging Sub‐Saharan African Migrants in Social and Health Studies in Australia: Research and Ethical Challenges
von: Andre M. N. Renzaho, et al.
Veröffentlicht: (2025)

Research Participant Bill of Rights: Clarifying the Role of Research Physicians
von: Mark A. Rothstein
Veröffentlicht: (2025)

Equitable Data Sharing in Collaborative Health Research in Sub‐Saharan Africa: A Translational Bioethics Perspective
von: Pamela Andanda, et al.
Veröffentlicht: (2025)

(Epistemic) Injustice and Resistance in Canadian Research Ethics Governance
von: Sarah Clairmont, et al.
Veröffentlicht: (2025)

Natural Language Processing in Clinical Research Recruitment: A Scoping Review Enriched with Stakeholder Insights
von: Lara Bernasconi, et al.
Veröffentlicht: (2025)

Mandating Evidence‐Based Informed Consent Practices: A Critical Engagement with IRB Leader Focus Group Findings
von: Meredith V. Parsons, et al.
Veröffentlicht: (2025)

Human Research Protection Training Requirements: Alternatives for Community Researchers at CTSA‐Funded Research Institutions
von: Emily E. Anderson, et al.
Veröffentlicht: (2025)

Undue Inducement and Disparate Impact: A Collectivist Account
von: Christopher Bobier
Veröffentlicht: (2025)

Pain Management Research in Prehospital Settings: The Pain of Exception from Informed Consent
von: Michael Linke, et al.
Veröffentlicht: (2025)

Reconsidering Open‐Ended Consent for Biospecimen and Health Record Research in the United States and Europe
von: Mark A. Rothstein, et al.
Veröffentlicht: (2025)

Building Ethical Foundations in Research: Adaptation of a Research Ethics Training Program for Adolescents
von: Angela K. S. Gummadi, et al.
Veröffentlicht: (2025)

Acceptability and Feasibility of Using Educational Incentives for Research Participation to Advance Antiracism
von: Barbara Green‐Ajufo, et al.
Veröffentlicht: (2025)

Investigating Moral Distress in Clinical Research Professionals—A Deep Dive into Troubled Waters
von: Elena Bosack, et al.
Veröffentlicht: (2025)

Policies for the Inclusion of Pregnant Women in Research: Results from an International and a US Study
von: Anne Drapkin Lyerly, et al.
Veröffentlicht: (2025)

Incorporating Gender‐Neutral Language in IRB Materials: Perceptions of IRB Professionals
von: Kevin L. Nellis, et al.
Veröffentlicht: (2025)

Translational Genomics and Community‐Driven Research in Australia
von: Fiona Russo, et al.
Veröffentlicht: (2025)

Bioethicists’ Perspectives on Ethical Research: Results of the “Views in Bioethics Survey”
von: Leah Pierson, et al.
Veröffentlicht: (2026)

Emergency Care Research and Exception from Informed Consent: Addressing the Spectrum of Capacity for Consent
von: Neal W. Dickert, et al.
Veröffentlicht: (2026)

Research with Refugee Populations in North America: Applying the NIH Guiding Principles for Ethical Research
von: Julie M. Aultman, et al.
Veröffentlicht: (2024)

The Ethical Case for Decentralized Clinical Trials
von: Kathryn Muyskens, et al.
Veröffentlicht: (2024)

Should Researchers Destroy Audio or Video Recordings?
von: David B. Resnik, et al.
Veröffentlicht: (2024)

Single IRB Review and Local Context Considerations: A Scoping Review
von: Stephanie R. Morain, et al.
Veröffentlicht: (2024)

Navigating University Openness in Research Policy Inconsistent with Indigenous Data Sovereignty: A Case Analysis
von: Molly Wick, et al.
Veröffentlicht: (2024)

Moving to the Middle Ground: Redefining Genomic Utility to Expand Understanding of Familial Benefit
von: Kyle B. Brothers, et al.
Veröffentlicht: (2024)

Rapid Review of Therapy Protocols for Public Health Emergencies
von: Bruce G. Gordon, et al.
Veröffentlicht: (2024)

Participant Misrepresentation in Online Focus Groups: Red Flags and Proactive Measures
von: Lesley Andrew, et al.
Veröffentlicht: (2024)

Digital Twins in Translational Research and Health Care: An Anthropological Perspective
von: Jennifer K. Wagner
Veröffentlicht: (2026)