New Guidance on Electronic Informed Consent
- PMID: 28115388
- DOI: 10.1158/2159-8290.CD-NB2017-008
New Guidance on Electronic Informed Consent
Abstract
The federal government has issued new guidance on the use of electronic tools to inform and obtain consent from potential participants in FDA-regulated research. The document answers common questions about how to present information to subjects and submit materials to regulators as part of new drug or device applications.
©2017 American Association for Cancer Research.
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