This section provides links to policies and other information that apply to DAIDS collaborators involved in the design, conduct, oversight, or management of DAIDS’ clinical research as described in the scope of each policy.
- Enrolling Children in Clinical Research PolicyPDF
- Good Documentation PolicyPDF
- Human Subjects Protection (HSP) and Good Clinical Practice (GCP) Training RequirementsPDF
- Requirements for Essential DocumentsPDF
- Requirements for Informed Consent FormsPDF
- Storage and Retention of Clinical Research Records PolicyPDF
- Information Sheet: Single Institutional Review Board RequirementsPDF