Institutional Review Board Procedures and Implications After the applied dissertation committee has approved the proposal and the IRB package, the student.

Slides:



Advertisements
Similar presentations
The Role of the IRB An Institutional Review Board (IRB) is a review committee established to help protect the rights and welfare of human research subjects.
Advertisements

Institutional Review Board Guidance.  Independent Ethics Committee  Ethical Review Board  Research Ethics Committee 2.
Evaluating Risk 1 IRB CELT Presentation Colleen Donaldson – IRB Administrator Julie Wilkens – IRB Coordinator.
FERPA and IRB: Implications for Testing Centers Judith W. Grant, Ph.D.,CIP NCTA Conference San Antonio, Texas August 6, 2009.
 Daylene Meuschke, Ed.D Barry Gribbons, Ph.D RP Conference: April 2, 2013.
Research Involving Human Subjects Review of Risk and Protection from Harm.

UTHSC IRB: A How-To Guide
Federalwide Assurance Presentation for IRB Members.
Research and AWC Faculty Seminar, February 19, 2009, Mary Schaal, M.Ed.
 Understanding the IRB Process University of Tennessee Health Science Center Institutional Review Board.
What you need to know about the Saint Leo IRB review process.
Help us Help you: IRB Policy Updates Susan Bankowski, MS, JD IRB Chair.
Michelle Groy Johnson Quality Improvement Officer Research Integrity Office Tough Love: Understanding the Purpose and Processes of Quality Assurance.
INSTITUTIONAL REVIEW BOARD HISTORY AND ETHICS. 2 Ethical History : Holocaust : Nuremburg Trials 1964: Declaration of Helsinki :
 The IRB application  The Review Process  Summary of Protocol  Appendixes  Informed Consent  Recruiting materials  Research Instruments  Other.
Human Subjects Research Cynthia Edmonds Director, Office of Research Support Committees.
RESPONSIBLE CONDUCT IN HUMAN SUBJECTS RESEARCH MARGARITA M. CARDONA DIRECTOR OF SPONSORED RESEARCH Institutional Review Board.
Collecting Data. Overview Approval (IRB) Prepare (protocol, practice) Recruit (getting subjects) Conduct (forms, practice)
The Institutional Review Board: A Community College Toolkit Dr. Geri J Anderson.
Office of Research Integrity and Compliance March 2011.
How to Successfully Apply to the IRB Richard Gordin, IRB Chair True Rubal, Administrator / Director For the Protection of Human Participants in Research.
The Linguistics Department Institutional Review Board Committee Silvina Montrul, chair Fred Davidson Irene Koshik Ryan Shosted September 22, 2008.
SUNY Oswego Human Subjects Committee Last Revised 10/28/2011.
Human Subjects Research at ASU An Overview. Overview Definitions Historical Framework Federal Guidelines Human Subjects Research at ASU.
Institutional Review Board Procedures and Implications After the applied dissertation committee has approved the proposal and the IRB package, the student.
Institutional Review Board Issues for Classroom Research Sharon McWhorter IRB Administrator, The University of Akron (With assistance from Phil Allen,
Western Oregon University INSTITUTIONAL REVIEW BOARD.
Welcome New IRB Members! Today we will discuss: Your Role in the IRB: What to Know The IRB Review Process Resources Human Research Protections.
NAVIGATING THE IRB PROCESS University Institutional Review Board California State University, Stanislaus.
IRB Process Overview Ling Wang IRB Representative Graduate School of Computer and Information Sciences.
TUN IRB: The Basics February 26, IRB Function Review human-subject research Ensure the rights & welfare of human subjects are adequately protected.
Human Research Ethics: Issues and Procedures Dr. Constance Jones Chair, Committee for the Protection of Human Subjects.
The IRB Process Southern New Hampshire University.
Paul Kelly Facility Research Compliance Officer for the Ralph H. Johnson VA Medical Center.
Senta Baker Sharon Moran IU Human Subjects Office Human Subjects Office IRB Submissions and KC Demostration School of Music November 13, 2015.
Conducting Research at Lincoln IRB/HRPP Policies, Procedures & Good Clinical Practices B Kanna MD, MPH, FACP Associate Program Director of Internal Medicine.
Paul Hryvniak MS, CIP Alyssa Speier, MS, CIP September 30, 2014 Student Human Research Education Session Tel:
Protecting Human Subjects in Research A Primer on Understanding the Scope, Purpose, and Process of the Kaplan University IRB Prepared by the Office of.
 What is an IRB and why do we need one at Western?  Who needs to submit proposals to the IRB?  If approved, how long is your proposal good for?  Is.
SoTL Research and the IRB Process Kathleen McKinney, Cross Chair in SoTL Nancy Latham, Campus IRB Executive Committee Phyllis McCluskey-Titus, SoTL Scholar.
THE INSTITUTIONAL REVIEW BOARD. WHAT IS AN IRB? An IRB is committee set up by an institution to review, approve, and regulate research conducted under.
Institutional Review Board (IRB) for Human Subjects.
Introduction to the HRPP and IRB Human Research Protection Program (HRPP) Office.
 The purpose of IRB is to ensure the rights of research subjects are protected  In accordance with the ethical standards of the U.S. Department of Health.
 The purpose of IRB is to ensure the rights of research subjects are protected  In accordance with the ethical standards of the U.S. Department of Health.
University Committee on Human Subjects (UCHS) Our contract with the Federal government is our “Federalwide Assurance” (FWA), and our FWA number is FWA
The Institutional Review Board (IRB) Brief Overview.
Tips for Success in Navigating the Human Subjects Protection System
Faculty Advisor Responsibilities
Introduction to the Human Research Protections Office (HRPO)
COCE Institutional Review Board Academic Spotlight
IRB BASICS Ethics and Human Subject Protections Summer 2016
Principal Investigator Responsibilities
How to Navigate IRB Paperwork.
Introduction to IRB (Institutional Review Board)
How to Navigate IRB Paperwork.
Understanding The Institutional Review Board Process
Multisite Human Subjects Research
IRB The purpose of IRB is to ensure the rights of research subjects are protected In accordance with the ethical standards of the U.S. Department of Health.
How to Navigate IRB Paperwork.
UW-Madison Central IRB Gateway
How to Navigate IRB Paperwork.
GSBM Presentation Updated
Overview of Process for GSEP Students
GPS IRB SPP Updated
GPS IRB SOL Updated
GPS IRB SIX STEPS Updated
I’m doing a project; how do I know if I need to go through the IRB?
SoTL Research and the IRB Process
Presentation transcript:

Institutional Review Board Procedures and Implications After the applied dissertation committee has approved the proposal and the IRB package, the student should forward a copy of the approved proposal together with the completed IRB submission package to the ARC for review. (See the ARC Web page, Navigating the IRB Process). NO RESEARCH STUDY ACTIVITY SHOULD TAKE PLACE BEYOND THE PROPOSAL STAGE UNTIL OFFICIAL NOTIFICATION HAS BEEN RECEIVED FROM THE ARC, INDICATING THAT THE PROPOSED RESEARCH STUDY MEETS THE UNIVERSITY’S IRB REQUIREMENTS.

Responsibilities of the IRB The purpose of the IRB is to guarantee that the welfare and rights of human subjects are adequately protected and informed consent given, if necessary. human subjects are not placed at unreasonable physical, mental, or emotional risk as a result of research. the researchers are qualified to conduct research involving human subjects. subjects are fully aware of the study’s parameters and what role they (and/or their data) play.

Additional Responsibilities of the IRB To ensure that ethical and safe research is conducted at Nova Southeastern University To protect NSU students and faculty To fulfill NSU requirements according to Federal-wide Assurances that guarantee the oversight and enforcement of federal regulations that protect human subjects involved in research

Types of IRB Reviews Exempt or Center Level Expedited Full All studies, regardless of the nature of the review, must be reviewed by IRB representatives prior to the beginning of research-related activities (e.g., asking friends and colleagues to participate constitutes a research activity).

Consequences of Not Obtaining IRB Approval Implementing your study again—starting over! Inability to use collected data Loss of funding Dismissal from FSEHS and NSU If in doubt, please contact the ARC IRB representatives to get the information before you begin research activities

How to Retrieve the Navigating the IRB Process Manual Visit the Applied Research Center Web site: Click “Academic Resources” Click “Online Guides” Review “Institutional Review Board” section

Required IRB Documents NSU IRB New Submission Form (requires student and committee chair signatures) Research Protocol (in detail) Administration Letter (from site where study will take place) Informed Consent/Assent forms (number of required consent forms may vary with each study) Informed Consent Form Checklist (one per consent form) Recruitment materials (e.g., flyers, brochures)

Required IRB Documents (Cont.) One copy of the approved proposal Data collection instruments Proof of Collaborative IRB Training Initiative (CITI) completion