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Informed Consent for Secondary Research under the New NIH Data Sharing Policy

Published online by Cambridge University Press:  19 October 2021

Abstract

The new NIH data sharing policy, effective January 2023, requires researchers to submit a data management and data sharing plan in their grant application. Expanded data sharing, encouraged by NIH to facilitate secondary research, will require informed consent documents to explain data sharing plans, limitations, and procedures.

Type
Columns: Currents in Contemporary Bioethics
Copyright
© 2021 The Author(s)

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Footnotes

About This Column

Mark A. Rothstein serves as the section editor for Currents in Contemporary Ethics. Professor Rothstein is the Herbert F. Boehl Chair of Law and Medicine and the Director of the Institute for Bioethics, Health Policy and Law at the University of Louisville School of Medicine in Kentucky. (mark.rothstein@louisville.edu)

References

These include the Data Sharing Policy, 68 Fed. Reg. 37369 (2003); Genomic Data Sharing Policy, 79 Fed. Reg. 51345 (2014); and NIH Policy on the Dissemination of NIH-Funded Clinical Trials Information, 81 Fed. Reg. 64922 (2016).Google Scholar
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Scientific Data: The recorded factual material commonly accepted in the scientific community as of sufficient quality to validate and replicate research findings, regardless of whether the data are used to support scholarly publications. Scientific data do not include laboratory notebooks, preliminary analyses, completed case report forms, drafts of scientific papers, plans for future research, peer reviews, communications with colleagues, or physical objects, such as laboratory specimens.” Id. at 68896-68897 (Section II).Google Scholar
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