Division of AIDS (DAIDS) Clinical Research Protocol and Informed Consent Development

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
  • Enrolling Children in Clinical Research Policy, Job AidPDF
  • Enrolling Children in Clinical Research Policy, Recommended LanguagePDF
• Good Documentation PolicyPDF
  • Appendix A Good Documentation Practice Job AidPDF
• Human Subjects Protection (HSP) and Good Clinical Practice (GCP) Training RequirementsPDF
• Requirements for Essential DocumentsPDF
• Requirements for Informed Consent FormsPDF
  • DAIDS Protocol/Sample Informed Consent Template—General UseDOC
• Storage and Retention of Clinical Research Records PolicyPDF
• Information Sheet: Single Institutional Review Board RequirementsPDF