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Robert A Lewis updated page 5.7 Obtaining Informed Consent from Non-English Speaking Persons, or Persons with Additional Needs or Vulnerabilities
23 hours ago

Robert A Lewis updated page 1.1 Human Research Protection Program (HRPP)
1 week ago

Robert A Lewis updated page 1.29 ClinicalTrials.gov Reporting
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Robert A Lewis updated page 8.7 Reporting Incidents to Institutional Officials and Federal Agencies
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Robert A Lewis updated page 6.4 Emergency Use of a Test Article
1 week ago

Robert A Lewis updated page 1.29 ClinicalTrials.gov Reporting
1 week ago

Robert A Lewis updated page 8.7 Reporting Incidents to Institutional Officials and Federal Agencies
1 week ago

Robert A Lewis updated page 6.4 Emergency Use of a Test Article
1 week ago

Robert A Lewis updated page 4.2 Research Involving Pregnant Women, Human Fetuses, and Neonates (Nonviable or of Uncertain Viability)
2 weeks ago

Robert A Lewis updated page 4.6 IRB Review of Research Involving Subjects with Impaired Decision-Making Capacity
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Robert A Lewis updated page 3.2 Data and Safety Monitoring
3 weeks ago

Robert A Lewis updated page 1.28 External Investigator Assurance
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Robert A Lewis updated page 4.6 IRB Review of Research Involving Subjects with Impaired Decision-Making Capacity
3 weeks ago

Robert A Lewis updated page 4.2 Research Involving Pregnant Women, Human Fetuses, and Neonates (Nonviable or of Uncertain Viability)
3 weeks ago

Robert A Lewis updated page 1.7 IRB Member, Consultant, Staff and Guest Conflict of Interest Identification and Management
1 month ago

Robert A Lewis updated page 1.5 Requirements for Research Conducted with International Sites
1 month ago

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5.7 Obtaining Informed Consent from Non-English Speaking Persons, or Persons with Additional Needs or Vulnerabilities

HRPP Policies and Procedures Section 5: Informed Consent

1.0 Purpose The purpose of this policy is to describe the Organization’s requirements for the pr...

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