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Informed Consent and Other Regulatory Docs

Event Details

Date
Thursday, October 7, 2010
Time
2:30-4 p.m.
Location
Description
A broad overview of the consent process: using the consent form wizard, written consent, oral consent, waiver of documentation of consent and assent for minors or those with diminished capacity. IRB reviewers look most closely at the consent form and other supporting documents that are provided to research participants. Learn what the regulations require, what the IRBs require and the most common errors.
Cost
Free

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