Clinical Research

Choose one of the following links:

Support researchers in performing their clinical research, including assistance with:

  • IRB and Regulatory Document Preparation
  • Protocol Development and Review
  • Contract and Budget Negotiation
  • Coverage Analysis Review
  • Clinical Research Coordinator Support
  • Registering your study with the CRO

Fully equipped facility to perform clinical research, including:

  • Nine exam rooms
  • Phlebotomy and sample collection
  • Participant interviews
  • Laboratory processing and shipment of samples
  • Registered Research Pharmacy
  • Many other services

Go to the IRB website for detailed information and to request IRB approval for your study.