TRAINING:
PROTECTION OF HUMAN RESEARCH SUBJECTS
NIH Policy Notice Published in NIH Guide - 6/5/2000 [Item Below Denoted by
Is Specifically Mentioned in this Notice as Meeting this Educational Requirement]
Frequently Asked Questions for the Requirement for Education on the Protection of Human Subjects (via NIH)
MUOT TRAINING MODULES
Research Ethics and Research Oversight: How We Got Where We Are (Dale Hammerschmidt, M.D., Medicine Grand Rounds, March 7, 2002)
NIH Office of Human Subjects Research Training Modules
Human Participants Protection Education for Research Teams (via NIH-NCI)
Other NIH Training Modules
Protection of Participants in Behavioral and Social Sciences Research (via NIH)
Clinical Research Training (via NIH Clinical Center)
SBIR/STTR: Human Subject Requirements (via NIH)
PHS Office for Human Research Protection (OHRP) Training Modules (3 Modules)
Human Subjects Assurance Training (Module Selection Screen)
Individual OHRP Assurance Training Modules as PDF Files:
Module 1: Federal Regulations & Institutional Responsibilities [For Investigators, IRB Members, & Institutional Administrators]
Module 2: Investigator Responsibilities & Informed Consent [Primarily for Investigators]
Module 2: Human Protections Program Administration & IRB Responsibilities [Primarily for Institutional Administrators & IRB Members]
Investigator 101 (Available on CD from IRB Office)
TRAINING MODULES FROM OTHER INSTITUTIONS
Patient-Oriented Research Training (via U. Penn) [username = guest, no password required]
Protection of Human Subjects in Research (via Indiana University)
Human Subjects Training (via Baylor College of Medicine)
Conducting Human Research (via Washington University - St. Louis)
Human Subjects Experimentation (via Univ. of California-Irvine)
Tutorial for Human Subjects Protection (via Kansas University Medical Center)
Children's Hospital of Philadelphia Training Modules
The History and Ethics of the Protection of Human Participants in Research
The Role of the Institutional Review Board
Scientific Integrity, Conflict of Interest, and Compliance
Good Clinical Practice in the Conduct of Research [FDA Form 1572 Pledges]
Human Subjects Protection Slide Presentations (via Columbia Univ.)
Human Subjects Protection Tutorial (via San Diego State Univ.)
Web-Based Seminar on Ethics of Research with Human Subjects (via Univ. of Indiana)
Ethical Issues in Human Subjects Research - Case Studies (via Univ. of Washington)
Protecting Human Subjects Guide (via Univ. of Minnesota)
Informed Consent Tutorial (via Univ. of Minnesota)
Human Subjects Research Ethics Tutorial (via Michigan State University)
Human Research Subjects Protection (via Jaeb Center for Health Research)
Responsible Conduct of Research - Human Subjects (via Univ. of Utah)
Protecting Human Research Subjects (via UCLA)
TESTS ON PROTECTION OF HUMAN RESEARCH SUBJECTS
IRB Training Quiz (via Oklahoma State Univ)
TRAINING SPECIFIC TO FDA REGULATIONS
Patient Misuse and Investigator Fraud in Clinical Trials: What Can Be Done? Part I (via FDA)
Whos in Charge Anyway? Responsibility in Todays Clinical Trial Environment (via FDA)
PHS Regulations
FDA Regulations