Safety Resources

Safety Reporting

DMID has centralized safety information gathered in all DMID-sponsored clinical trials involving greater-than-minimal risks in human subjects. This page, DMID Clinical Research Policies and Standard Procedure Documents, provides information on DMID’s Centralized Pharmacovigilance Program and links to Policies, SAE Reporting Guidelines and Forms, and Toxicity Tables.


DMID Safety Oversight – This page provides information on the function and responsibilities of DMID’s Safety Oversight Boards, Committees and Monitors. Links to forms and guidelines can be found near the bottom of the page.