Clinical Services

Clinical Development Program

Compliance Resources LLC

Compliance Resources has a network of experienced project managers and senior clinical research associates to assist with your clinical development program. Our expertise is most effective when applied during the initiation of a clinical study to ensure that adequate training has taken place and management systems are in place before the trial is underway. We implement clinical trial management tools and systems that are designed to promote the development of clinical study report sections while the trial is being conducted. These tools and processes lead to the completion of the clinical study report in a timely manner once the study has been completed.

Our services include:

  • Generation or Review of Study Training Materials
  • Conduct of Investigator Meetings
  • Study Initiation Visits
  • Periodic Site Visits
  • Termination Site Visits
  • Co-Monitoring Visits
  • Drug Accountability Visits
  • FDA Readiness Program for Clinical Sites
  • Clinical Study Report authorship
Compliance Resources LLC