Introduction to IRB (Institutional Review Board)

Slides:



Advertisements
Similar presentations
Is it Research?. Is It Research? 2 Elements –The project involves a systematic investigation –The design (meaning goal, purpose, or intent) of the investigation.
Advertisements

Evaluation and Human Subjects Research Julie M. Aultman, Ph.D. Chair, Institutional Review Board Associate Professor, Family and Community Medicine Northeast.
IRB SUBMISSION PROCESS FOR SHB STUDIES Version 9/18/2013.
Human Subjects Protections, Concepts, and Procedures Office of Research and Sponsored Programs Tom Lombardo, Ph.D., Director, Research Integrity & Compliance.
Institutional Review Board Guidance.  Independent Ethics Committee  Ethical Review Board  Research Ethics Committee 2.
DO NO HARM IRRB Presentation Purposes Responsibilities Processes NLU IRRB Home page.
IRB 101: Introduction to Human Subject Research
Research Involving Human Subjects Review of Risk and Protection from Harm.
Cooperative Research IRB Brownbag, 3/4/08. ISU Policy Cooperative research projects are those projects which involve more than one institution. The official.
IRB Basics Helen Panageas New York University School of Medicine Institutional Review Board Portion of slides courtesy of Suzanne M. Smith, University.
Human Subjects Research Dr. John S. Irvine Chairperson, NMSU Institutional Review Board for Human Subjects Research
Human Investigation Committee  Is it research?  If yes, does it involve human subjects?  If yes, can it be exempt?  If no, will a Request for.
RESEARCH COMPLIANCE: Health Sciences Institutional Review Board.
Cornell Evaluation Network The Use of Human Participants in Research Office of Research Integrity and Assurance ~ May 14, 2007.
How To Begin Doing Human Subjects Research Teri Bycroft Associate Director of Human Subjects Research.
Avoiding the Pitfalls of an IRB Submission Chris Ayres Chair, Institutional Review Board Social & Behavioral Science & Chair, Department of Kinesiology,
April 2011 Conducting Research at SPC Approval Process and Procedures Center of Excellence for Teaching and Learning.
INSTITUTIONAL REVIEW BOARD HISTORY AND ETHICS. 2 Ethical History : Holocaust : Nuremburg Trials 1964: Declaration of Helsinki :
Responsible Conduct of Research: IACUC & IBC Office of Regulatory Research Compliance.
Committee on Human Research Processes Clinical Translational Research Fellowship Program Curriculum Core.
The Human Subjects Institutional Review Board Workshop Part 1: An Introduction to Human Subjects Research Ethics and the IRB Process Presented by Alena.
Protecting Human Participants in Your Research and Classroom Projects NAU Institutional Review Board
RESPONSIBLE CONDUCT IN HUMAN SUBJECTS RESEARCH MARGARITA M. CARDONA DIRECTOR OF SPONSORED RESEARCH Institutional Review Board.
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.
Investigators’ Responsibilities in Conducting Human Subjects Research Dept. of Regulatory Affairs April 18, 2012.
Human Subjects Research at ASU An Overview. Overview Definitions Historical Framework Federal Guidelines Human Subjects Research at ASU.
Dustin Yocum, MA Institutional Review Board University of Illinois HUMAN SUBJECTS RESEARCH.
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.
Brown Bag Series on Research Faculty Protection of Human Subjects in Research February 10, 2012 Gerberding Hall 142, University of Washington.
Human Subjects Review: Policies and Procedures. Why A Human Subjects Review? It is the policy of this University that all researchers undertaking studies.
NAVIGATING THE IRB PROCESS University Institutional Review Board California State University, Stanislaus.
AAHRPP ACCREDITATION (Association for the Accreditation of Human Protection Programs)
CUNY Human Research Protection Program (HRPP) School of Professional Studies April 18, 2013
Paul Kelly Facility Research Compliance Officer for the Ralph H. Johnson VA Medical Center.
Institutional Review Board “IRB Snapshot”. IRB Team Annabelle Casas—Institutional Coordinator for Research Review (extension 7939) Irene Holguin—Grants.
Paul Hryvniak MS, CIP Alyssa Speier, MS, CIP September 30, 2014 Student Human Research Education Session Tel:
Office of Research Integrity and Protections (ORIP) Tracy Cromp Director orip.syr.edu.
© 2015 Marketo, Inc. Marketo Proprietary and Confidential Page 1 Investigators’ Responsibilities in Conducting Human Subjects Research Office of the Vice.
Protecting Human Subjects in Research A Primer on Understanding the Scope, Purpose, and Process of the Kaplan University IRB Prepared by the Office of.
Human Subjects Research at Mines Colorado School of Mines New Faculty Orientation November 20, 2015.
Research Ethics Office of Research Compliance. Responsible Conduct of Research (RCR) Covers 9 content areas –Animal Subjects (IACUC) –Human Subjects (IRB)
Doing IRB Right … Together JOHN POTTER, OD, MA Chair, Institutional Review Board.
University Committee on Human Subjects (UCHS) Our contract with the Federal government is our “Federalwide Assurance” (FWA), and our FWA number is FWA
Welcome to the Butler Institute for Research & Scholarship (BIRS) Presented by Taura Edwards, BIRS Director Kanti Crain, Research Compliance Officer.
Understanding Compliance IRB (The Institutional Review Board) Kanti Crain, MA, CIP Research Compliance Officer Butler Institute for Research and Scholarship.
COCE Institutional Review Board Academic Spotlight
University of Central Florida Office of Research & Commercialization
Conducting Human Subjects Research
Research with human participants at Carnegie Mellon University
SOU Institutional Review Board
Tarleton State University
IRB – Human subjects research incoming staff orientation 2017
The Institutional Review Board: Who, What, When, Where, Why, and How
Conducting Human Subjects Research
University of Central Florida Office of Research & Commercialization
What Every Harvard LMA Student Investigator Should Know
SOU Institutional Review Board
IRB – Human subjects research incoming staff orientation 2018
What are the Role & Purview of the IRB?
Conducting Human Subjects Research
What Every Harvard LMA Student Investigator Should Know
What types of research are exempt and ohrp guidance on exemptions
CUNY Human Research Protection Program (HRPP)
Everything You Wanted to Know about UOPX IRB
Demystifying the IRB Process: An Interactive Conversation with QIP
Research with Human Subjects
Research Compliance: Protections for Research Subjects
Presentation transcript:

Introduction to IRB (Institutional Review Board) Presented by Kanti Crain, MA, CIP Research Compliance Officer Butler Institute for Research and Scholarship Oct 2015

Research Compliance Ensure that research activities are in compliance with the federal regulations, state law and the institution's policy. IRB (Institutional Review Board) IACUC (Institutional Animal Care and Use Committee) IBC (Institutional Biosafety Committee)

IRB (Institutional Review Board) What is an IRB? Any board formally designated by an institution to review, to approve the initiation of, and to conduct periodic review of research involving human subjects. The primary purpose of such review is to assure the protection of the rights and welfare of the human subjects What has to be reviewed by the IRB? Any research that involves Human Subjects What is Research? A systematic investigation, including research development, testing and evaluation, designed to develop or contribute to generalizable knowledge What are Human Subjects? A living individual about whom an investigator (whether professional or student) conducting research obtains: • Data through intervention or interaction with the individual, or • Identifiable private information

IRB continued … How to submit an application? Email to IRB@butler.edu Or JH 109 Room D What is the submission and review process? The duration of approval is based on the level of risks: Exempt – No Expiration Expedited – Typically 1 year Full Board - Typically 1 year Cooperative Research Review – depends on the level What are the requirements for an IRB submission? Principle Investigator: Full-time Faculty/ Staff All investigators: Complete CITI (https://www.citiprogram.org/) Complete and submit the application form and the research documents (Consent, recruitment materials, survey list etc).

IRB Flowchart Received by BIRS Pre Review Review Approval

More Information http://legacy.butler.edu/research-scholarship/compliance/overview/ Contact Kanti Crain: 940-6424 or kcrain@butler.edu Jordan Hall 109 D