WINTHROP-UNIVERSITY HOSPITAL INSTITUTIONAL REVIEW BOARD (IRB) IRB Meeting Calendar, Deadline Dates and IRB Membership List Educational Requirements in Human Subjects Protections Ethical Codes and Good Clinical Practices Policies and Guidelines Federal Agencies IRB Submission Forms Frequently Asked Questions Glossary (in lay terms) Guidance for Research Participant Contact IRB Article Tools  Print this page  Email this page

IRB Submission Forms Below are forms that must be used when submitting items for review by the Winthrop IRB: Form 253 - Application for Exempt Projects (Updated) Form 252 - Expedited Review Application (Updated) Waiver of Consent and Authorization Form 251 - Application for Review of a Research Project - Full Board (Updated) Decendents Form Short Consent Form For Non-English Speaking Subjects (New) Short Consent Form WUH Form 254 - Modification Request Form (Updated) Form 256 - Reportable Events Submission Form (Updated) Continuing Review Form Scientific Merit Review Form Termination Form FDA 1572 Form FDA Form 310 (Protection of Human Subjects Assurance Identification/IRB Certification/Declaration of Exemption) Form 266 - Notification of Emergency Use of a Test Article Report (Subsequent to Use)

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