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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