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Research Protections Office

Research Protections Office
Human Subjects Research
Vertebrate Animal Research
Biosafety Oversight
News and Events
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RPO A-Z

Research Protections Office

RPO A-Z

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A

Acronym List
Add a Commercial Farm for Purposes of Research or Teaching (IACUC)
Amendment Review Forms (IRB)
Amendment Form (IBC)
Animals in Research
Animal Use Protocol Amendment Form (IACUC)
Animal Use Protocol Form (IACUC)

B

Biosafety Oversight
Biosafety Oversight Protocol Form (IBC)
Biosafety Oversight Research Manual

C

Calendar of Events
CITI Program Training
Clinical Research Center
Clinical Trials Registration Information - Last updated February 19, 2015 (PDF)
Compliance and Privacy Services
Committee Login - Restricted Access
Consent Forms
Contact Us
Continuing Review Form (IACUC)
Continuing Review Forms (IRB)
Cooperative Research (Single IRB)

D

Does the Project Require IRB Review and Approval?

E

Electronic Submission Guide (InfoEd)
Enviromental Health and Safety Office
Ethics and Compliance Reporting 877-310-0413

F

Federalwide Assurance (FWA) and IRB Registration
Forms Library
Frequently Asked Questions

G

General FAQs
Good Clinical Practice (GCP)

H

HIPAA
HIPAA Research FAQs
How to create a separate account through CITI
How to Log Into InfoEd and Navigate a Protocol Record
How to make sure you have a UVM Net ID
How to Prepare Documents
How to Submit a Protocol Request to the RPO Office
Human Subjects Research

I

IACUC Training Completions (requires UVM NetID login)
IBC Training Completions
Incident Report Form (IBC)
InfoEd Delegation Request Form
Information Technology and Security
IRB Policies and Procedures
IRB Research Analyst
IRB Training Completions

J

J

K

Key Personnel or PI Change (IACUC)
Key Personnel or PI Change (IBC)
Key Personnel Review Forms (IRB)

L

List of University of Vermont - CITI Program course(s)

M

Meeting Dates and Submission Deadlines

N

News and Events
News Archives
Not Research Determination Self-Service Tool

O

Occupational Health and Safety Forms
Office of Animal Care Management
Office of Clinical Trials Research
Optional Consent Module

P

Plain Language Medical Dictionary
Post Approval Monitoring

Q

Q

R

Regulatory Changes
Request for InfoEd Access Form
Research Integrity
Research Protections Office

S

Safety Review Forms (IRB)
Single IRB
Special Notice – Common Rule Delay
Special Notice – Consent Form Changes
Special Notice – Instructor Assurance
Sponsored Project Administration
Standard Operating Procedure (IBC)
Steps to Develop and Submit a Protocol Application
Student Class Project Guidelines

T

Top 10 Obstacles to IRB Approval
Training Requirements

U

UVMClick
UVM Medical Center
UVM Medical Center Integrity and Compliance

V

Vermont Cancer Center
Vermont Center for Clinical and Translational Science
Vertebrate Animal Research
Vertebrate Animal Research Manual
Vice President for Research

W

Waiver Request
Western IRB
What Is the Definition of a Clinical Trial for Registration Purposes?

X

X

Y

Y

Z

Z

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