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Step 1. Is your project considered research?
Step 2. Does your research involve human subjects?
Step 3. Is your Human Subjects research exempt from the…
Step 4. Is your research considered to be "UW Research"?
Home
Human Subjects Division
About Us
Clinical Trials
Clinical Trials Registration and Reporting
Clinical Trials Registration and Reporting Questions and Answers
How to Post a Consent Form to a Federal Website
How to Register a Clinical Trial
How to Report Clinical Trial Results
How to Update a Clinical Trial Record
Contact HSD
Do I Need IRB Review?
Step 1. Is Your Project Considered Research?
Step 2. Does Your Research Involve Human Subjects?
Step 3. Is Your Human Subjects Research Exempt from Regulations?
Step 4. Is Your Research Considered to be “UW Research”?
HSD Data and Reports
HSD Training and Education
HSD Required Training
Zipline Online Help Library
Additional Education and Resources
Is the UW IRB the Right IRB?
General Information
How to Ask For a Non-UW IRB
Identify the Correct IRB
Meeting Schedule for the IRBs
Research Participants
Revised Common Rule
Newsletter Schedule
Questions and Answers
Resources
The Changes
Vocabulary of the Revised Common Rule
Which Studies and When
Single IRB
UW is a Participating Site
UW is the Lead or Coordinating Site
Single Patient Emergency Use
Special Topics
Consent, Assent and Waivers
Data and Safety Monitoring
Deception
Delayed Onset Human Research (DOHR)
Engagement
Humanitarian Use Devices (HUDs)
International Research
Just-in-Time and IRB Review
Minimal Risk (Expedited) Review
Repositories
Subject Privacy, Confidentiality and Identifiable Data
Study IRB-Related Activities
Apply for Review
Modify the Approved Study
Renew Your IRB Approval
Report Events and New Information
Close Your IRB Application
Zipline
Zipline Conversions
Zipline Release Notes