Human Subjects Research Guidance Library

If you have a question about a topic not listed here, please contact the main office by email at researchcompliance@uoregon.edu or phone at (541) 346-2510 for assistance. For your convenience, RCS has compiled a list of commonly used Human Subjects Research definitions.

Jump to Research Administration Portal (RAP) Guidance Index

Topic Index

A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z

A

• Appealing the CPHS/IRB Decision
• Approval-In-Principle (AIP)
• Audio Recording, Video Recording, and/or Photography

B

• Broad Consent

C

• Changes to the Common Rule
• Clinical Trials
• Closing your study
• Collaborations and Reliance Arrangements 
• Compensation for Participation in Research
• Continuing Review

D

• Determine if your project requires IRB review

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E

• Event Reporting (RNIs)
• Exempt Self-Assessment Tool Instructions

F

• Frequently Asked Questions (FAQs)

G

• Genetic Research

H

• HIPAA and Human Subject Research
• Human Physiology Emergency Procedures

I

• Informed Consent
• Initial Review
• Investigator Responsibilities

M

• Minors in Research
• Modification Review (Amendments) (also see Modifying an Existing Protocol)

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P

• Participant Pools (Marketing, SOJC, and Psychology/Linguistics)
• Passive Parental Consent
• Permissions and Approvals
• Principal Investigator Eligibility, Faculty Advisors, and Research Personnel Requirements
• Prisoners in Research

Q

• Qualtrics - UO site licensed survey software and data collection tool

R

• Radiation in Research
• Recruitment
• Required Training (CITI)
• Research Plan
• Risks to Participants

S

• Safety Monitoring, Participant Privacy and Confidentiality of Data
• Student-Led Research and Faculty Advisors

T

• Translations and Translated Materials
• Transporting Participants

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Research Administration Portal (RAP) Guidance Index

A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | Q | R | S | T | U | V | W | X | Y | Z

A

• Accessing your studies
• Ancillary Review - Instructions for students to add a faculty advisor
• Ancillary Review - Instructions for faculty advisors to approve student led research
• Ancillary Review - Instructions for the Research Medical Director and others
• Approval in Principle (AIP)
• Attachments - Instructions on where to attach study materials

C

• Create a single-site study
• Create a multi-site study where UO is the relying IRB
• Create a multi-site study where UO is the reviewing IRB
• Creating a pSite (RAP Instructions)
• Continuing Review/Study Closure (RAP Instructions)

F

• Frequently Asked Questions

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M

• Migrated Studies
• Modify Study (RAP Instructions)
• Modify an External IRB Study where UO is the relying IRB

Q

• Quick Reference - Primary Contacts and PI Proxies
• Quick Reference - Study Funding Sources
• Quick Reference - Study Team Members

R

• Report new information (RNI)
• Responding to clarification request or modification required notification
• RAP Quick Reference - Guest List
• RAP Quick Reference - Units (Other Study Information section).pdf
• RAP Quick Reference - Continuing Review for External IRB Study Guidance for Researchers.pdf

S

• Submit Study Instructions (RAP)

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