Skip to main content
The University of Iowa
Search
Human Subjects Office
About Us
Contact Us
Report a Concern
Federalwide Assurance
Introduction to IRB
Regulations & Policies
Belmont Report
State of Iowa Information
HIPAA
Privacy Board Responsibilities
HIPAA Privacy Rule Info & Resources
Policy Archives
International Research
GDRP
eResearch Application
IRB Fees
Site Map
Get Started
Roles & Responsibilities
Principal Investigators
Student PIs & Faculty Advisors
Research Team Members
Delegates
Research Course Instructors
Instructors
Advisors
Institutional Review Boards
IRB 01
IRB 02
Research at the VAHCS
VA Principal Investigator Guide
IRB 04
Emergency Use of an Investigational Drug or Device
Forms Not Available in HAWKIRB
Evaluation to Sign an Informed Consent Document for Research
Protocol Outline
Specimen or Data Repository Procedures at UI
Tips
Recruitment
Mass Email Requests
Off Campus Research
International Research
CITI Training
Department of Defense
Responsible Conduct of Research
Good Clinical Practice
Faculty Advisors
Do I Need IRB Approval?
Other Research Review
Other Committee Review Relationships
Research Billing Compliance (RBC)
RBC Policy Updates
Holden Comprehensive Cancer Center Protocol Review and Monitoring Committee
Conflict of Interest in Research Committee
Institutional Biosafety Committee
Medical Radiation Protection Committee
Cooperating Schools Program
Pharmacy and Therapeutics (P&T) Committee
Investigator-Dispensed Drug Study Form
VAHCS Research & Development Committee
Nursing Research Committee
Training Requirements
ClinicalTrials.gov
ClinicalTrials.gov Working Group
UI Investigator's Guide\IRB Standard Operating Procedures
Important 2018 Changes
Use of Gadolinium in Research
FDA Site Inspection Guidance
UI IRBs
Department of Defense (IRB 04)
IRB Overview
HawkIRB Information
Modifying Attachments in HawkIRB
Central & External IRBs (Single IRB of Record)
SMART IRB
WIRB
WIRB Submission
UI WIRB Fees
2012 Fees
WIRB Review Process
WIRB Consent Documents
UI/WIRB Consent Document Template
Post-Approval Submissions
WIRB Archive
WIRB as a Central IRB
Great Plains Collaborative
NCI CIRB
StrokeNet
Quorum
Community Based Research (CBR)
CBR Continuum
CBR Eligibility
Guidance Ebooks
Get Help
Training Sessions
IRB ICON Course for Researchers
Office Hours
Small Group Presentations
IRB Connection HSO Newsletter
IRB Advisor
Frequently Asked Questions
IRB-03 VA Review
Human Subjects Protections Certification
What to Expect During the IRB Review Process
Getting the IRB Application Started
Status of a Submitted Application
IRB Approval
Modifying an Approved IRB Application or Materials
Continuing Review of IRB-Approved Research
Withdraw or delete a HawkIRB Application
Closing a Study
Record of Consent
Delegates in HawkIRB
HawkIRB Delegate Permissions Instructions
HIPAA FAQS
Research Subject Payment and Compensation
Consent Process (Including Informed Consent Documents)
Short Form Consent Document (Short Form) FAQ
Short Form Consent Instructions
List of Translators in Iowa City-Coralville
Mailed Consent Process: Handling corrections
New Faculty/Staff Survey
Faculty/Staff Orientation
Submit to IRB
IRB Review Process
Types of Review
IRB Determinations
HawkIRB System
New Project
About Assurances
Approval Stamp - Saving Attachments on Mac
Creating a Consent Document
Record of Consent
Umbrella Projects
Modification
Continuing Review
Study Closure
Reportable Events
IND/Outside Safety Reports
Human Subjects Research Determinations
External IRB
Calendar of Events
Info for Research Participants and the Public
Rights as a Research Subject
New OHRP Material
Participating in Research
Research Studies at UI
Research Studies at VA
Become an IRB Member
Human Subjects Research in the News
Archived Regulatory News & Updates
Archived Items on the HSO Website
Policies, News & Updates
Learn More
UI IRB Metrics
For IRB Members
IRB Member Materials
Compliance Monitoring
You are here
Home
»
Submit to IRB
»
IRB Review Process
IRB Determinations
Types of Review
IRB Determinations