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IRB-HSR
>
Managing Protocol After Initial Approval
> Informed Consent
Informed Consent
Background
Elements of Consent Form
Informed Consent Considerations for Certain Types of Studies
Re-consenting Requirements
Altering or Waiving Elements of Informed Consent/Waiver of Consent
Waiver of Documentation of Informed Consent
Consenting Subjects who do not Read, Speak or Understand English Informed
Maintenance of Informed Consent Documentation
Research Exempt from Informed Consent
Assessing Subject's Understanding
Who Can Obtain Consent from Potential Subjects?
Use of consent & assent forms to enroll minors
For more information see Learning Shot
"The Informed Consent Process for Clinical Research "
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Last Modified: 08-Feb-2008 11:20:27 EDT
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