Sentral

 

WHAT SENTRAL CLINICAL RESEARCH SERVICES PROVIDES

  • Rent for utilized space
  • Personnel required to complete the study
  • Document management
  • Identification and Recruitment of appropriate studies
  • Contracting for studies
  • Billing and collection for study-related services
  • Patient compensation for participation
  • Advertising for clinical trial participants
  • Chart review to identify appropriate study candidates
  • Documentation of study results
  • Interactions (as necessary) with sponsor monitors and other regulatory personnel
  • Completion and submission of IRB-required documents
  • Training in Good Clinical Practices and Human Subject Protection
  • Quality Assurance/Quality Control
  • Clinical trial management software
  • Support and presence during FDA audits

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