Conduct Resources

Conduct of all DF/HCC clinical trials must follow all DF/HCC Standard Operating Procedures (SOPs). The Office of Human Research Studies (OHRS) and Office of Data Quality (ODQ) have created numerous Guidances and Information Sheets to assist researchers in the management of their studies.Serious Adverse Event Reporting and Continuing Review requirements are essential elements of trial conduct. The Clinical Operations Committee (CLINOPS) provides a forum for research management at the DF/HCC member institutions.

This section provides useful resources for protocol conduct.