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Human Subjects Division
Contact HSD
Getting Started
Application Forms
Topic-Based Guidance
Ancillary Review
Certificate of Confidentiality (CoC)
Consent
Delayed Onset Human Research (DOHR)
Department of Energy
Ethical Principles
Exempt Research
Expanded Access Guidance
FDA Regulated Research
Humanitarian Use Device Guidance
International Research
IRB Review Resources
Is it Research?
Just-in-Time and IRB Review
Protected and Vulnerable Populations
Recruitment
Research Inquiries
Return of Individual Results
Specific Federal Agency Requirements
Subject Payment
Human Subjects Training
HSD Required Training
Zipline Online Help Library
HSD Tutorials and Videos
Additional Education and Resources
Reliance on a Non-UW IRB
General Information
How to Ask For a Non-UW IRB
Identify the Correct IRB
Transfers of IRB Oversight and PI Institutional Affiliation Changes
Single IRB
UW is a Participating Site
UW is the Lead or Coordinating Site
UW IRB as a Single IRB
ClinicalTrials.gov
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
Study IRB-Related Activities
Report Safety/Compliance Events
For Research Participants
Zipline
Zipline Campus Training Site