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Creating Informed Consent Forms for Clinical Trials: A Primer

Event Details

Date
Thursday, February 3, 2011
Time
1-2:30 p.m.
Description
A clear, easy-to-understand consent form is an essential part of an effective informed-consent process. Review regulatory requirements for informed consent, learn about tools and resources available to help create a consent document and deal with special consent procedures, and get tips for composing clear and readable consent forms. Intended for study teams who write their own consent forms for clinical trials.
Cost
Free

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