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AIDS Research and Human Retroviruses|September 23, 2006
Post-trial access to tested interventions: the views of IRB/REC chair, investigators, and research participants in a multinational HIV/AIDS studyChristine Pace, Christine Grady, David Wendler, et al.Journal of the American Medical Informatics Association : JAMIA|June 12, 2018
Using mobile location data in biomedical research while preserving privacyDaniel M Goldenholz, Shira R Goldenholz, Kaarkuzhali B Krishnamurthy, et al.Vaccine|April 29, 2014
Placebo use in vaccine trials: recommendations of a WHO expert panelAnnette Rid, Abha Saxena, Abdhullah H Baqui, et al.Health Economics, Policy, and Law|September 27, 2023
We need to talk about values: a proposed framework for the articulation of normative reasoning in health technology assessmentVictoria Charlton, Michael DiStefano, Polly Mitchell, et al.The American Journal of Bioethics : AJOB|November 18, 2017
Reframing Consent for Clinical Research: A Function-Based ApproachNeal W Dickert, Nir Eyal, Sara F Goldkind, et al.Annals of Emergency Medicine|December 29, 2015
Confronting Ethical and Regulatory Challenges of Emergency Care Research With Conscious PatientsNeal W Dickert, Jeremy Brown, Charles B Cairns, et al.The American Journal of Bioethics : AJOB|August 26, 2015
Broad Consent for Research With Biological Samples: Workshop ConclusionsChristine Grady, Lisa Eckstein, Ben Berkman, et al.Journal of the International AIDS Society|December 15, 2021
Ending the evidence gap for pregnancy, HIV and co-infections: ethics guidance from the PHASES projectAnne Drapkin Lyerly, Richard Beigi, Linda-Gail Bekker, et al.BMJ Global Health|February 10, 2025
Observational research in epidemic settings: a roadmap to reformEmily E Ricotta, Fausto A Bustos Carrillo, Samuel Angelli-Nichols, et al.Learning Health Systems|October 31, 2025
Disentangling informing participants from obtaining their consentPatricia Pearl O'Rourke, Joseph Ali, Judith Carrithers, et al.Pageof 20