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CTTI

Clinical Trials Transformation Initiative

Recommendations for Informed Consent

Posted on June 8, 2021February 5, 2025 by Hannah Faulkner

Recommendations for Informed Consent

This entry was posted in Informed Consent, Informed Consent, Recommendations, Safety, Study Design, Study Operations. Bookmark the permalink.

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← Sample Tiered Informed Consent Model
Recommendations for Strengthening the Investigator Site Community →

DISCLAIMER: CTTI encourages the use of all materials listed on this site in the pursuit of improving the clinical trials enterprise. Our recommendations, tools, meeting summaries, and more are available to the public for free. We do ask that you acknowledge the source whenever using or referencing CTTI materials. Read our Citation Policy. 

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