Skip to main content
University of Washington
Research
Contact Us
About Office of Research
Announcements
UW Home
Quick Links
MyResearch Project Lifecycle
Plan/Propose
Plan/Propose Overview
Develop Hypothesis/Question
Select Funding Source
Conduct Literature Search
Sponsor Requirements
Recruit Team
Budget
Facilities and Resources
Write Proposal
Submit Proposal
Tools
MyResearch
SAGE
Zipline
More Tools
Setup
Setup Overview
Sponsor Requirements
Facilities and Resources
Financials
Subawards
Compliance Requirements (Non-Financial)
Records and Documentation
Methods
Collaborations
Data Collection
Tools
MyResearch
SAGE
Zipline
More Tools
Manage
Manage Overview
Financials
Compliance Requirements (Non-Financial)
Facilities and Resources
Collect Data
Analyze Data
Subawards
Award Changes
Reporting
Tools
MyResearch
SAGE
Zipline
More Tools
Closeout
Closeout Overview
Financials
Subawards
Equipment and Materials
Reporting
Dissemination of Results
Data Sharing
Records Retention
Tools
MyResearch
SAGE
Zipline
More Tools
Resources
Support Offices
Browse
Forms and Templates
Policies, Procedures and Guidance
Announcements
Glossary
FAQs
Popular Resources
Funding Opportunities
Grant Information Memoranda (GIMs)
Institutional Facts and Rates
Research Stats & Rankings
New to UW Research
Tools
MyResearch
SAGE
Zipline
More Tools
Collaboration
Connect to Expertise
Find Research Expertise
Research Centers and Institutes
Resources for Collaboration
Interdisciplinary Resources
Guidance for NIH Institutional Training Grants
Collaborative Proposal Development Resources
Establish a Research Center or Institute
Shared Research Facilities and Resources
Tools
MyResearch
SAGE
Zipline
More Tools
Compliance
Compliance Overview
Compliance
Training
Training Overview
Research Training Overview
Collaborative for Research Education
Required Research Training
Research Administration Learning
HSD Training and Education
MyResearch Training Transcript
Human Subjects Division
hsdinfo@uw.edu
206.543.0098
UW Research
Menu
MyResearch Project Lifecycle
Plan/Propose
Setup
Manage
Closeout
Resources
Collaboration
Compliance
Training
Home
UW Research
Human Subjects Division
Do I Need IRB Review?
Single Patient Emergency Use
Do I Need IRB Review?
Human Subjects Division
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”?
Step 5. Is the UW IRB the Right IRB?
External IRB Review of UW Research
Existing Reliance Agreements
Industry Sponsored Research
HSD Data and Reports
HSD Training and Education
HSD Required Training
Zipline Online Help Library
Additional Education and Resources
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
Ask for Non-UW IRB
Zipline
Zipline Conversions
Zipline Release Notes
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"?
Step 5. Is the UW the right IRB?
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”?
Step 5. Is the UW IRB the Right IRB?
External IRB Review of UW Research
Existing Reliance Agreements
Industry Sponsored Research
HSD Data and Reports
HSD Training and Education
HSD Required Training
Zipline Online Help Library
Additional Education and Resources
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
Ask for Non-UW IRB
Zipline
Zipline Conversions
Zipline Release Notes