Clinical Research Resources

Below are the most common forms and policies that affect investigators and employees conducting clinical research projects. The list is not exhaustive and other forms and policies not listed here may or may not impact your particular project.

Clinical Trial Management Services   A Guide to Submitting and Maintaining Studies

Clinical Trials Standard Operating Procedures – SOPs

HCMC Clinical Services for Research

Office for Human Subjects Research / IRB

Office for Education & Quality in Clinical Research

Teleconference Call Access

If you do not see the information you are looking for please contact Carla Erickson at (612-873-6341) or Pat Engstrand at (612-873-5300).