Lasting Ethical Implication in Research: The Tuskegee Experience Sapana Panday Widener University.

Slides:



Advertisements
Similar presentations
Ensuring Ethical Use of Quality Improvement Mary Ann Baily, PhD HIVQUAL US Advisory Committee Meeting August 24, 2008.
Advertisements

Adapted from ISEF webpage Society for Science and the Public “Roles and Responsibilities of students and adults” Roles and Responsibilities of students.
Ethical regulations for health research involving human subjects in Cambodia By Chap Seak Chhay, MD, MPH, MHPEd Public Health and Health Professions Educator.
By: Ronald F. White, Ph.D. Professor of Philosophy College of Mount St. Joseph.
UH employees and students who conduct research involving human subjects are required to obtain approval from the Committee on Human Studies (CHS). John.
DO NO HARM IRRB Presentation Purposes Responsibilities Processes NLU IRRB Home page.
Cooperative Research IRB Brownbag, 3/4/08. ISU Policy Cooperative research projects are those projects which involve more than one institution. The official.
PPA 691 – Seminar in Public Policy Analysis Lecture 1d – The Belmont Report.
Detectives in the Classroom - Investigation 2-3: What's Wrong with This Picture? What's Wrong with This Picture?
© HRP Associates, Inc. Ethics & Regulation of Human Subjects Research Jeffrey M. Cohen, Ph.D., CIP President, HRP Associates, Inc.
Ethics in Research involving Human Subjects Dr. Walid S. Abdelkader Head of Preventive Medicine and Primary Care Division IMC Feb
RESEARCH DURING DISASTERS Robert J. Levine, MD Professor of Medicine and Lecturer in Pharmacology; Director: Donaghue Initiative in Biomedical and Behavioral.
1 Wheaton College INSTITUTIONAL REVIEW BOARD (IRB)
A History of Human Research Protections and Institutional Review Boards Roger L. Bertholf, Ph.D. Associate Professor of Pathology Chair, University of.
Regulatory Authority Governing Clinical Trials Anthony J. Minisi, MD Director, Cardiology Fellowship Program.
What makes Clinical Research Ethical? Dr Enoka Corea Co-secretary, ERC Faculty of Medicine, Colombo.
INSTITUTIONAL REVIEW BOARD HISTORY AND ETHICS. 2 Ethical History : Holocaust : Nuremburg Trials 1964: Declaration of Helsinki :
HUMAN RESEARCH HISTORICAL PERSPECTIVE. Objectives Identify the history events that lead to the development of principles, regulations, and guidance.
1 HUMAN RESEARCH PROTECTIONS Daniel R. Vasgird, PhD, CIP Office of Research Compliance West Virginia University (304)
The QA/QI Process Human Research Subjects Protection Human Investigation Committee Tracy Rightmer, JD, CIP Compliance Manager.
© 2009 Cengage Learning. All Rights Reserved. Clinical Research.
Institutional Review Board for Human Subject Research: Does Your Research Need One? Merle Rosenzweig Michael Unsworth.
Protecting Human Participants in Your Research and Classroom Projects NAU Institutional Review Board
Frederick G More, DDS, MS Professor New York University New York, NY, USA July 2009University of Haiti.
RESPONSIBLE CONDUCT IN HUMAN SUBJECTS RESEARCH MARGARITA M. CARDONA DIRECTOR OF SPONSORED RESEARCH Institutional Review Board.
Legal & Ethical Issues. Objectives At the completion of this session the participant will be able to: ◦ Describe the ethical principles associated with.
The Institutional Review Board: A Community College Toolkit Dr. Geri J Anderson.
Eugenics Movement Nuremberg Code Declaration of Helsinki WWII – Time Line for Human Subject Research and.
Office of Research Integrity and Compliance March 2011.
Institutional Review Board (IRB) What is our Purpose and Role for Ethical Research.
TERRENCE F. ACKERMAN, PH.D. PROFESSOR OF BIOETHICS CHAIR, UTHSC IRB.
The ethical conduct of research with human participants Nancy E. Kass, ScD Department of Health Policy and Management Johns Hopkins Berman Institute of.
Human Subjects Research at ASU An Overview. Overview Definitions Historical Framework Federal Guidelines Human Subjects Research at ASU.
How Can You Recruit for Your Project Frederick G. More, DDS, MS IRB Chairman NYU School of Medicine HRPP PI Lecture Series.
The Pharmaceutical Industry and International Clinical Research: One Company’s Approach Michael Clayman, M.D. Vice President, Lilly Research Laboratories.
The Ethics of Research on Human Subjects. Research Activity on Human Subjects: Any systematic attempt to gain generalizable knowledge about humans A systematic.
Consent Procedures. What is Informed Consent? Consent by a patient to a surgical or medical procedure or participation in a clinical study after achieving.
Mid – Late 1970’s Emergence of recombinant DNA technology Concerns among both scientific community and general public:  Public health and safety  Environmental.
NAVIGATING THE IRB PROCESS University Institutional Review Board California State University, Stanislaus.
Applicability of principles Reidar K. Lie, MD, PhD Department of Clinical Bioethics, NIH and University of Bergen, Norway.
Identifying current and potential ethical challenges and Dilemmas in HIV prevention Research Ethics in clinical research: challenges linked.
What Institutional Researchers Should Know about the IRB Susan Thompson Senior Research Analyst Office of Institutional Research Presented at the Texas.
© 2011 Pearson Prentice Hall, Salkind. The Importance of Practicing Ethics in Research.
WELCOME to the TULANE UNIVERSITY HUMAN RESEARCH PROTECTION OFFICE WORKSHOP for SOCIAL/BEHAVIORAL RESEARCH (March 2, 2010) Tulane University HRPO Uptown.
Betsy Ripley, MD, MS Professor of Medicine Division of Nephrology VCU IRB Senior Chair VCU Clinical Research Compliance Officer Associate Chair Faculty.
Basics of Research Ethics Prepared by: R. Bortolussi MD FRCPC Professor Pediatrics Dalhousie University Workshop Google images.
Is public "Health” & “Pride” influence by? Health & Pride Nationalism Public Opinion PropagandaJustice Presentation by Maria C Alvarez May 6 th, 2015.
Ethical Issues Carolyn R. Fallahi, Ph. D.. Ethical treatment of children Laws: All U.S. states have laws regulating contact between psychologists and.
Beyond Regulations: Ethical Considerations in Research
All About the Institution Review Board! Jennifer A. Jones, M.S. Jessica P Lauren E. Ewaniuk M.Ed ED 510 Fall 2011.
Chapter 5 Ethical Concerns in Research. Historical Perspective on Ethics Nazi Experimentation in WWII –“medical experiments” –Nuremberg War Crime Trials.
The Importance of Practicing Ethics in Research.  Summarize why it is important to practice ethical research.  Describe the basic principles of ethical.
0 Ethics Lecture Research. ACADEMY OF OPHTHALMOLOGY Disclosures  The speaker has no financial interest in the subject matter of this.
Doing IRB Right … Together JOHN POTTER, OD, MA Chair, Institutional Review Board.
Ethics in Research A class discussion. What is Ethics in Research? and Why is it Important?
Class 9 Jeff Driskell, MSW, PhD
Ethics in Social Psychology
SOU Institutional Review Board
The Institutional Review Board: Who, What, When, Where, Why, and How
Protection of Human Subjects In Research
Research Clinical Audit Service Evaluation
Characteristics of research
Ethical Principles of Research
SOU Institutional Review Board
American Public Health Association
Ethical Considerations for Pediatric Clinical Investigations
Social Responsibility and Business Ethics
Ethical issue in medical research.
Research with Human Subjects
Presentation transcript:

Lasting Ethical Implication in Research: The Tuskegee Experience Sapana Panday Widener University

History of Bioethics Commissions – The Advisory Committee on Human Radiation Experiments The National Commission for the Protection of Human Subjects of Biomedical Behavioral Research 2001–09

The Belmont Report The Belmont report is a statement of basic ethical principles and guidelines surrounding the conduct of research with human subjects. The report was published in the Federal Register, and reprints provided upon request. This was to ensure that it was readily available to scientists, members of Institutional Review Boards, and Federal employees. ohsr.od.nih.gov/guidelines/belmont.html

Boundaries between Practice and Research The distinction between practice and research is blurred especially when they occur together. ▫ Practice: interventions that are designed solely to enhance the well-being of an individual patient and that has a reasonable expectation of success. ▫ Research: an activity designed to test an hypothesis, with the potential to generate generalizable knowledge. Practice and research may be carried on together when trying to evaluate the safety and efficacy of a therapy. ohsr.od.nih.gov/guidelines/belmont.html

Basic Ethical Principles ohsr.od.nih.gov/guidelines/belmont.html

Applications ohsr.od.nih.gov/guidelines/belmont.html

Common Rule ori.hhs.gov/education/products/ucla/chapter2/page04b.htm

“…it became the standard declaration of ethical principles for research not only in the United States, but in most of the rest of the world.” Robert J. Levine, MD Professor of Medicine Yale University Co-Author, Belmont Report