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
- NIAID HIV Language Guide
- Requirements for Essential Documents
- Requirements for Informed Consent Forms
- Storage and Retention of Clinical Research Records Policy
- DAIDS Guidance on the Use of Gender-Inclusive HIV Research Practices
- DAIDS Memo Regarding New DAIDS Requirements: Informed Consent Process
- DAIDS Memo Regarding Timing of Consent and Re-Consent with Updated IRB/EC/RE-Approved Informed Consent Forms
- DAIDS Memo Regarding the Revised Common Rule and Implementation
- DAIDS Memo Regarding an Update on the Single IRB Requirement
- DAIDS Memo Requesting Exceptions from NIH OD for the sIRB Requirement