546 Improving the compliance of informed consent documentation for expanded access patients

Objectives/Goals: The informed consent (IC) process is similar between clinical trials and expanded access (EA), which allows clinical use of investigational products outside studies. Physicians face unique barriers to IC in clinical environments. This project assesses IC documentation, identifies p...

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Bibliographic Details
Main Authors: Elias Samuels, Misty Gravelin, Ellen Champagne, Dorsa Haj Ghaffari, Jeanne Wright
Format: Article
Language:English
Published: Cambridge University Press 2025-04-01
Series:Journal of Clinical and Translational Science
Online Access:https://www.cambridge.org/core/product/identifier/S205986612401118X/type/journal_article
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