Adult Clinical Capabilities

  • Recruitment and enrollment of adult subjects in clinical studies
  • Perform follow-up visits, specimen collection and processing
  • Clinical evaluations, evaluation of adverse events
  • Administration of study product (if needed).
  • Remote surveillance of subjects using internet access (cohort studies)
  • Coordination with participating practice sites (Primary Care Research Network - PBRN)
  • Regulatory affairs, preparing IRB documentation and filings
  • Case reporting, reporting of adverse events.
  • Support for monitoring groups
  • Coordination with study sponsors/DMID
  • Vaccine Research Unit