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Editorials |

U.S. Research Regulations: Do They Reflect the Views of the People They Claim to Protect?U.S. Research Regulations

John D. Lantos, MD
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This article was published online first at www.annals.org on 14 April 2015.

From Children's Mercy Hospitals and Clinics, Kansas City, Missouri.

Disclosures: Disclosures can be viewed at www.acponline.org/authors/icmje/ConflictOfInterestForms.do?msNum=M15-0632.

Requests for Single Reprints: John D. Lantos, MD, Center for Bioethics, Children's Mercy Hospitals and Clinics, 2401 Gillham Road, Kansas City, MO 64108; e-mail, jlantos@cmh.edu.

Ann Intern Med. 2015;162(10):731-732. doi:10.7326/M15-0632
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In this issue, Cho and colleagues report results of a survey examining attitudes about risk and preferences for notification and consent for research among U.S. adults. The editorialist discusses the survey findings and emphasizes that research participants should have a voice in shaping the current regulatory system for clinical research.

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