The CRU functions as a “one stop” operation and provides all the resources, support services and trained personnel to facilitate the conduct of ICH-GCP/FDA compliant clinical trials. These include the following:

  • Clinical Research Nursing

  • Contracts and Budgets

  • Data Management and research record management

  • Investigational Drug Services

  • Participant recruitment and retention 

  • Regulatory Affairs

  • Research Study Management