Clinical Terms of Award (CTA): Describes the researchers roles and responsibilities for both the awardee and the program officer.
Clinical Terms of Award (CTA) Guidance Document: Guidance for compliance with NIAID Clinical Terms of Award.
Regulatory File Document Guidelines (PDF)
Source Documentation Standards for Clinical Research (PDF)
DMID Translation Policy (PDF) and tools (MS Word)
DMID Requirements for Staff Training in Good Clinical Practice and Human Subjects Protections (PDF)
DMID Requirements for IRB/IEC Review of Human Subjects Research (PDF)
Development of Criteria for Volunteer Participation in DMID Clinical Research (PDF)
Expanded Distribution of Clinical Research Endpoint Data (PDF)
Unblinding Individual Participants in DMID Clinical Research (PDF)
Gender/Minority Reporting Guidelines (PDF): Instructions for reporting women and minority inclusion in clinical research
DMID Clinical Research Policy Development, Review and Approval for NCRS Documents (PDF)
Staff Training in Good Clinical Practice and Human Subjects Protections (PDF)
Last Updated January 05, 2013