Develop IRB/ethics protocols for human subjects research. Use when: (1) Planning studies involving humans, (2) Preparing IRB applications, (3) Ensuring ethical compliance, (4) Addressing informed consent.
Create comprehensive ethical protocols for institutional review board approval.
1. Study Purpose
2. Study Design
3. Participant Selection
4. Risks and Benefits
5. Informed Consent
6. Privacy and Confidentiality
7. Compensation
Minimal Risk: No greater than daily life More than Minimal: Requires full board review
Version: 1.0.0