Institutional Review Board Materials

 

The Institutional Review Board (IRB) is a committee that protects human subjects involved in research by reviewing and monitoring research activities to ensure that subjects are treated fairly and risks are minimized.

 

 

POLICIES AND REGULATIONS

 

Regulations of the Institutional Review Board of the Madlyn and Leonard Abramson Center for Jewish Life

 

Financial Conflict of Interest Policy

 

DHHS Final Guidance Document on Financial Relationships in Research Involving Human Subjects: Guidance on Human Subject Protection

 

Research Funded by Federal Agencies: Title 45, Part 46, Protection of Human Subjects (45CFR46)

 

Belmont Report

 

 

FORMS

 

The forms below are Word documents. After opening a form, select 'File' and 'Save As' to save a copy on your own computer. Please print completed forms to submit. Forms are due to the IRB administrator by the first Monday of the month that the application is to be reviewed.

 

The Office of Human Research Protection has designed the following aids to determine if a study involves human subjects and must be reviewed by an Institutional Review Board: Human Subject Decision Charts

 

 

Initial Review Forms

 

Application for Initial Review - Polisher Research Institute Staff

 

Application for Initial Review - Other Abramson Center for Jewish Life Staff

 

Application for Initial Review - Outside Investigators

 

 

Continuation Review Form

 

Application for Continuation Review

 

 

Other Forms

 

Request for Change in Protocol

 

Adverse Event Form

 

Protocol Close-Out Form

 

 

Conflict of Interest Forms

 

Conflict of Interest Affidavit - Investigator

 

Conflict of Interest Affidavit - Non-Investigator

 

 

 

TRAINING AND TOOLS

 

Informed Consent Guidelines

 

The Signatory Official, Human Protections Administrator and IRB Chair are required to complete the following training:
Office of Human Research Protection: Human Subject Assurance Training

 

IRB Chair, committee members, investigators, and key research personnel are required to complete the following tutorial:
National Institutes of Health: Human Participant Protections Education for Research Teams

 

**Please submit a certificate of completion to Susanne Morganstein.

 

 

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