'Human research protections' presentation slideshows

Research Ethics, Compliance, IRB, & IACUC Presented by: Joanne Muratori & Patria Davis

Research Ethics, Compliance, IRB, & IACUC Presented by: Joanne Muratori & Patria Davis. Objective Review history, role, and function of the Institutional Review Board Review federal definition of human subjects research and levels of review

925 views • 78 slides

Engagement in Human Research & Multi-Site Studies

622 views • 52 slides

642 views • 47 slides

Institutional Review Board (IRB) Overview for Medical, Behavioral and Educational Research

Institutional Review Board (IRB) Overview for Medical, Behavioral and Educational Research. Jack Medendorp M.S., B.S.N., CIP. Office of Regulatory Research Compliance Drexel University. DISCUSSION POINTS. Regulatory Oversight What is Research? Levels of IRB Review

697 views • 43 slides

Protecting Human Subjects In Social-Behavioral-Educational Research: Working with the IRB

450 views • 36 slides

Fraud and Misconduct in Clinical Trials

Fraud and Misconduct in Clinical Trials. Dr Jane Barrett Consultant Pharmaceutical Physician MedicoLegal Investigations Ltd www.barrettconsultancy.com www.medicolegal-investigations.com. Learning outcomes. To understand the Background of fraud and misconduct

2.36k views • 36 slides

PROTECTING HUMAN SUBJECTS IN Social-Behavioral-Educational RESEARCH: Working with the IRB

PROTECTING HUMAN SUBJECTS IN Social-Behavioral-Educational RESEARCH: Working with the IRB. Lisa Shickle , MS Analyst, VCU Massey Cancer Center Member, Exempt Panel E and Panel B Monika S. Markowitz, Ph.D. Director, Office of Research Compliance & Education

530 views • 35 slides

International Human Subjects Research

International Human Subjects Research. Edward E. Bartlett, PhD International Human Research Liaison Office for Human Research Protections September 20, 2006. Outline. Overview of the Office for Human Subjects Research 2. Trends in international research

491 views • 28 slides

Significant Events

Presented by Georgia Institute of Technology Institutional Review Board Presented by Melanie Clark, CIP Associate Director Office of Research Integrity Assurance. Nuremberg Code 1947 U.S. Scandals Henry Beecher: "Ethics and Clinical Research" Public Health Service Policy Adopting IRBs

418 views • 28 slides

A History of Human Research Protections and Institutional Review Boards

A History of Human Research Protections and Institutional Review Boards. Roger L. Bertholf, Ph.D. Associate Professor of Pathology Chair, University of Florida IRB-03. The Nuremberg Trials. The International Military Tribunal (1945) The Doctors Trial (1946) The Nuremberg Code (August, 1947).

517 views • 23 slides

Alternative Sources of Human Embryonic Stem Cells

Alternative Sources of Human Embryonic Stem Cells. Ethics Matters. Lawrence M. Hinman, Ph.D. Professor of Philosophy Co-Director, Center for Ethics in Science & Technology University of San Diego Larry at EthicsMatters dot net June 5, 2009. Introduction: The Issue.

423 views • 22 slides

Breaking Through: M aking the Move from Management to Leadership

Breaking Through: M aking the Move from Management to Leadership. Suzanne (Sue) Rivera, Ph.D. Associate VP for Research Case Western Reserve University. Menu. Research Administration= Career Options for professional growth in RA Techniques for career planning

308 views • 21 slides

DO NO HARM

DO NO HARM. NLU IRRB Home page. IRRB Presentation. Purposes Responsibilities Processes. NLU IRRB Home page. IRRB Purposes. Assure that research follows ethical principles and guidelines. Assist the investigator in examining ethical implications of their research. NLU IRRB Home page.

524 views • 20 slides

Running an IRB on a Shoe String Budget: the Essentials of Operating an IRB

Running an IRB on a Shoe String Budget: the Essentials of Operating an IRB. Dr. R. Kirk Jonas Ms. Carolyn Strong, CIM,CRA Chair , Institutional Review Board Research Compliance Coordinator University of Richmond James Madison University rjonas@richmond.edu strongcd@jmu.edu

347 views • 20 slides

DO NO HARM

DO NO HARM. NLU IRRB Home page. IRRB Presentation. Purposes Responsibilities Processes. NLU IRRB Home page. IRRB Purposes. Assure that research follows ethical principles and guidelines. Assist the investigator in examining ethical implications of their research. NLU IRRB Home page.

355 views • 20 slides

Privacy and Confidentiality

342 views • 16 slides

John E. Sidle, M.D. February 23, 2006

299 views • 15 slides

Post Approval Monitoring Program

Post Approval Monitoring Program. by Louisa Gay Post Approval Monitoring Officer. What is Post Approval Monitoring Why should we do this Who will be involved Logistics Questions. Discussion Areas.

338 views • 15 slides

Chapter 5

Chapter 5. Ethical Concerns in Research. Basics in Ethics. Examples of unethical conduct in research Regulation of research and protection of research participants Scientific misconduct in reporting. Examples of unethical conduct. Nazi Germany experimentation during World War II

241 views • 13 slides

Common Rule and FDA Regulation Comparison

539 views • 13 slides