skip to main content
R&I division news
Quicklinks
Search
Apply
Research & Innovation
Go where knowledge leads
×
Quicklinks
University Tools
MYNEVADA
WEBCAMPUS
EMAIL ACCESS
INTERFOLIO
NEVADABOX
WORKDAY
ZOOM LOGIN
Academic resources
ACADEMIC ADVISING
ACADEMIC CALENDAR
COLLEGES & SCHOOLS
COURSE CATALOG
LIBRARY
NAVIGATE
Campus resources
CAMPUS MAP
EMPLOYEE DIRECTORY
HUMAN RESOURCES
PARKING
POLICE SERVICES
SERVICES FOR STUDENTS
STUDENT HEALTH CENTER
Information for
CURRENT STUDENTS
FACULTY & STAFF
PARENTS
ALUMNI
×
Search
Search www.unr.edu
Search
Popular Searches:
MyNevada
WebCampus
Housing
Research Integrity & Security
Research & Innovation | Where big ideas ignite.
Program Areas
Training
Contact Us
Menu
Program Areas
Human Research
General IRB Info
Human Research Protection Policy Manual
Policy Manual Definitions
Browse the definitions of technical terms in the Policy Manual
Quickstart Guide for Researchers
International Research
Research in Schools (K-12)
University Student Participants
Veterans Affairs Research
Clinical Research Resources
Clinical Trials Project Life Cycle
Clinical Trials Study Management
Data Safety & Monitoring
Sample Data Safety & Monitoring Plan Outline
Clinical Trials Contract & Budget
Regulatory Resources
Clinical Trial Requirements
Clinical Trials Investigator-initiated Research
Clinical Trial Registration FAQs
HIPAA and Human Subjects Research
Obtaining Human Research Data Under HIPAA
Quality Assurance Review
Consent Process Aids
Revised Common Rule requirements for informed consent
Creating Recruitment Materials
(Current Page)
For IRB Members
Completing a First-rate Review
For Research Participants
¿Debo participar en un estudio científico?
Information for research participants translated in Spanish
Institutional Animal Care and Use Committee
Institutional Biosafety Committee
Conflict of Interest
Disclosure Instructions
Procedures
Outside Compensated Services
COA Request Instructions
Reviewing Requests
Navigating COI and Related Regulations
Financial Conflicts of Interest
External Relationships
Paid Travel
Impacts on Students
Conflict of Interest Training
Responsible Conduct of Research
Research Misconduct
Research Security
U.S. Export Controls
Overview of Regulations
Policies and Procedures
Research Compliance
International Shipping
Foreign Workers and Visitors
Restricted Party Screening
Licensing
Recordkeeping Requirements
Reporting Violations
Protecting Electronic Data During Travel
Laptop Loan Program
Deemed Exports
Publicly Available, Public Domain, Open Source
Educational Information
Fundamental Research Exclusion
International Travel & Data Protection
Export Controls Training
Effort Reporting
Effort Certification
Working with Salary Caps
Video Tutorials
Training
HIPAA training
Responsible Conduct of Research training
IRBNet
How to Register in IRBNet
Contact Us
Research & Innovation
Go where knowledge leads
Announcement:
The federal administration has enacted a number of Executive Orders that have implications for federal proposals and awards.
View more information on research activity impacts.
University Homepage
/
Research Integrity
/
Program areas
/
Human research
/
Information for IRB members
Menu
Program Areas
Human Research
General IRB Info
Human Research Protection Policy Manual
Policy Manual Definitions
Browse the definitions of technical terms in the Policy Manual
Quickstart Guide for Researchers
International Research
Research in Schools (K-12)
University Student Participants
Veterans Affairs Research
Clinical Research Resources
Clinical Trials Project Life Cycle
Clinical Trials Study Management
Data Safety & Monitoring
Sample Data Safety & Monitoring Plan Outline
Clinical Trials Contract & Budget
Regulatory Resources
Clinical Trial Requirements
Clinical Trials Investigator-initiated Research
Clinical Trial Registration FAQs
HIPAA and Human Subjects Research
Obtaining Human Research Data Under HIPAA
Quality Assurance Review
Consent Process Aids
Revised Common Rule requirements for informed consent
Creating Recruitment Materials
(Current Page)
For IRB Members
Completing a First-rate Review
For Research Participants
¿Debo participar en un estudio científico?
Information for research participants translated in Spanish
Institutional Animal Care and Use Committee
Institutional Biosafety Committee
Conflict of Interest
Disclosure Instructions
Procedures
Outside Compensated Services
COA Request Instructions
Reviewing Requests
Navigating COI and Related Regulations
Financial Conflicts of Interest
External Relationships
Paid Travel
Impacts on Students
Conflict of Interest Training
Responsible Conduct of Research
Research Misconduct
Research Security
U.S. Export Controls
Overview of Regulations
Policies and Procedures
Research Compliance
International Shipping
Foreign Workers and Visitors
Restricted Party Screening
Licensing
Recordkeeping Requirements
Reporting Violations
Protecting Electronic Data During Travel
Laptop Loan Program
Deemed Exports
Publicly Available, Public Domain, Open Source
Educational Information
Fundamental Research Exclusion
International Travel & Data Protection
Export Controls Training
Effort Reporting
Effort Certification
Working with Salary Caps
Video Tutorials
Information for IRB members
General IRB information
IRB meeting schedule and information
IRB review fees
Levels of IRB review
General IRB information
IRB member resources
Belmont Report
Completing a first-rate review: Your responsibilities as an IRB reviewer
DHHS Policy Index
DHHS Decision Charts
Expedited Review Categories
Federal OHRP Educational Videos
Title 21 CFR Part 50 (FDA)
Title 21 CFR Part 56 (FDA)
Title 45 CFR Part 46 (DHHS)
