| IRB Administration, Authority and Responsibility |
Metro Health Human Research Protection Program |
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Research Involving Human Subjects |
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Review of Research By A Convened IRB |
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Metro Health IRB Authority and Purpose |
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Human Subject Protection and Education Training |
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The Instutional Official – Signatory Authority and HRPP Responsibility |
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IRB Reciprocity and Authorization Agreements for Cooperative Research Activities |
| Conflict of Interest in Research |
Conflict of Interest in Human Subject Research |
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Conflict of Interest in Research Disclosure Form |
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Conflict of Interest – IRB Members & IRB Administrative Staff |
| IRB Submission, Communication and Reporting |
Modification of Approved Human Research Application Requirements |
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Humanitarian Use Device Application Requirements |
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IRB Submission Requirements |
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Initial Human Research Application Requirements |
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Continuing Review Application Requirements |
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Unanticipated Problems & Adverse Event Reporting Requirements |
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Emergency Use of a Test Article Notification Requirements |
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| Informed Consent in Human Research |
Required Elements of Informed Consent in Research |
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Informed Consent for Non-English Speaking Subjects |
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Minor Assent for Participation in Research |
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Parental Permission for Minor Participation in Research |
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Waiver or Alteration of Informed Consent |
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Process and Documentation of Informed Consent |
| Research Conducted in Special Populations |
Adults With Diminished Decision Making Capacity |
