- Chapter 1 - Types of Research: Human Subjects Research Vs. Not Human Subjects Research
- Chapter 2 - Roles and Responsibilities of the Principal Investigator
- Chapter 3 – Obtaining and Preparing Required Documents for IRB Initial Review
- Chapter 4 - Writing Your Consent Document
- Chapter 5 - Submitting Your Initial Review
- Chapter 6 - Things To Do After IRB Approval But Before Starting Enrollment
- Chapter 7 - Conducting Your Study
- Chapter 8 - Subject Withdrawal from Research
- Chapter 9 - Reporting Research Related Events or New Information to the IRB
- Chapter 10 - Protocol Modifications
- Chapter 11 - Continuing Reviews (CR)
- Chapter 12 - Study closures (routine)
- Chapter 13 - Conducting Research With Special Populations
- Chapter 14 - FDA Regulated Research
- Chapter 15 - International Research
- Reference Links
Overview
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