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Ethics & Human Research|March 28, 2023
Remnant Blood Quantification: Informing the Definition of Minimal Risk in Clinical ResearchAdam L Gottula, Sara Constand, Sandra Cabrera, et al.
Ethics & Human Research|May 23, 2020
Why Challenge Trials of SARS-CoV-2 Vaccines Could Be Ethical Despite Risk of Severe Adverse EventsNir Eyal
Ethics & Human Research|September 8, 2021
Creating a Research Ethics Consultation Service: Issues to ConsiderHolly A Taylor, Kathryn M Porter, Erin Talati Paquette, et al.
Ethics & Human Research|September 8, 2021
IRB Decision-Making about Minimal Risk Research with Pregnant ParticipantsAmina White, Christine Grady, Margaret Little, et al.
Ethics & Human Research|December 31, 2025
Pain Management Research in Prehospital Settings: The Pain of Exception from Informed ConsentMichael Linke, Francis X Guyette, Jason McMullan
Ethics & Human Research|December 31, 2025
Policies for the Inclusion of Pregnant Women in Research: Results from an International and a US StudyAnne Drapkin Lyerly, Renee Muthakana, Aliyah Webster, et al.
Ethics & Human Research|June 21, 2020
Pregnant Women in Trials of Covid-19: A Critical Time to Consider Ethical Frameworks of Inclusion in Clinical TrialsRuth Farrell, Marsha Michie, Rachel Pope
Ethics & Human Research|May 21, 2021
Stakeholder Experiences with the Single IRB Review Process and Recommendations for Food and Drug Administration GuidanceAmy Corneli, Carrie B Dombeck, Kevin McKenna, et al.
Ethics & Human Research|March 14, 2025
Stakeholder Views on Novel Consent Forms for an Acute Stroke TrialCandace D Speight, Opeolu M Adeoye, S Iris Davis, et al.
Ethics & Human Research|January 3, 2025
Investigating Moral Distress in Clinical Research Professionals-A Deep Dive into Troubled WatersElena Bosack, Dawn Bourne, Elizabeth Epstein, et al.
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