DIVISION of RESEARCH

Comprehensive Clinical Research Unit

Clinical Trials & Staff

A chief objective of the CCRU is to provide leadership and support for clinical trials conducted in the region and for the clinical research staff that supports these trials.  The CCRU supports FDA-regulated and non FDA-regulated trials, including:

  • Industry-sponsored IND and IDE trials
  • Federally-sponsored trials
  • Investigator-initiated clinical trials
  • Humanitarian device exemption trials (HDE)
  • Expanded/new indication trials
  • Post-marketing trials