mybonsecours
IRB policies and procedures
Purpose and Authority
Limitations of Research Activities within the Bon Secours Richmond Health System
New Protocols
Revisions/Amendments to Protocols
Continuing Review
Closures
Review of Unanticipated Problems and Internal Deaths
Obtaining and Documenting Informed Consent of Subjects who do not speak English
Protocol Deviations
Disapproval, Suspension, or Termination of Investigation
Authorization Agreements with External Institutions and/or Investigators
Exemption from IRB Review
Humanitarian Use Devices
Vulnerable Population: Children
Treatment Use of an Investigational New Drug (IND)
Emergency Use of an Investigational New Drug
Investigational Drug Use in Patients Entering a Second Institution
Compassionate Use
Investigational Device Review
Emergency Use of Unapproved Medical Devices
