Making clinical trials more patient-centered using digital interactive e-consent tools
Research participants are required give their consent to participate in clinical trials and non-exempt government-funded studies. The goal is to facilitate participant understanding of the intent of the research, its voluntary nature, and the potential benefits and harms. Ideally, participants make...
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| Format: | eBook |
| Language: | English |
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Research Triangle Park, NC
RTI International
October 2019, 2019
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| Series: | Occasional paper
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| Online Access: | |
| Collection: | National Center for Biotechnology Information - Collection details see MPG.ReNa |
Table of Contents:
- Includes bibliographical references