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 Policy
- Good Documentation Policy
- Human Subjects Protection (HSP) and Good Clinical Practice (GCP) Training Requirements
- Requirements for Essential Documents
- Requirements for Informed Consent Forms
- Storage and Retention of Clinical Research Records Policy
- NIAID HIV Language Guide
- Information Sheet: Single Institutional Review Board Requirements