Guidance: Test Articles in Research
- General
- Frequently Asked Questions
- Cooperative Research
- Non-local IRB Review
- Continuing Review After Study Approval
- Sponsor - Investigator - IRB Interrelationship
- Foreign Clinical Studies, Acceptance of
- Charging for Investigational Products
- Recruiting Study Subjects
- Payment to Research Subjects
- Screening Tests Prior to Study Enrollment
- Informed Consent, A Guide to
- Use of Investigational Products When Subjects Enter a Second Institution
- Exception from Informed Consent Requirements for Emergency Research
- "Off-Label" and Investigational Use Of Marketed Drugs, Biologics, and Medical Devices
- Drugs and Biologics
- Medical Devices
- FDA Operations
- Guidance for the Content of Premarket Submissions for Software Contained in Medical Devices
