Documents
Document Details
| Last Updated | 07/12/2010 |
|---|---|
| Version | 1.30 |
| Filesize | 825 KB |
| Audiences | HSD Staff, IRB Member, Research Participant, Researcher |
| Doc Type | Procedure |
| Last Updated | 07/12/2010 |
|---|---|
| Version | 1.30 |
| Filesize | 825 KB |
| Audiences | HSD Staff, IRB Member, Research Participant, Researcher |
| Doc Type | Procedure |
| 
Purpose
This procedure describes how researchers can provide subjects with a description of the reasonably foreseeable risks of harm or discomforts associated with the proposed research, as part of the consent process.