Clinical Trials

Beaufort’s clinical trial management services are supported by a highly qualified team of diagnostic and medical device experts. Our proven track record in managing both domestic and international clinical trials from beginning to end sets the foundation of a lineup of industry-leading services. We will fully manage and provide strategic assistance for every phase of your clinical trial. Or, we will provide one or more stand-alone solutions as a functional service provider to complement your internal staff.

We Provide:

  • Study and protocol design and review
  • Case report form (CRF) design and development
  • Informed consent development and review
  • Clinical investigator evaluation, qualification and selection
  • Clinical or laboratory site identification, qualification and initiation
  • Clinical trial management and coordination
  • Selection, training and management of therapeutically qualified Clinical Research Associates (CRAs)
  • Trial Master File (TMF) creation and management
  • Institutional Review Board (IRB)/Ethics Committee (EC) submission support
  • Medical and safety monitoring
  • Conduct of investigator meetings
  • Database development and management
  • Statistical analysis and review
  • Sample size calculations and power analysis
  • Interim and final reporting
  • GCP audits and training


Read case studies of how Beaufort has helped clients meet their Clinical needs.