Clinical Research Management for Sponsors/CROs


SPIRITT offers medical device and pharmaceutical Sponsors/CROs a comprehensive list of services including:


  • Clinical Study Development and Execution
    • Project Management
    • Clinical Investigational Plan Design and Development
    • Protocol Development
    • Site Management
    • Data Management
      • Patient-Informed Data Collection
      • Database Development and Management
      • Data Analysis and Reporting
    • Safety Management
      • Adverse Events, Serious Adverse Events, and Unanticipated Adverse Device Effects
      • Medical monitoring
      • Data Safety Monitoring Board/Clinical Events Committee Activities
    • Monitoring
    • Institutional Review Board/Ethics Committee Submissions and Approvals
    • Clinical Study Report Writing
    • Clinical Contracting/Agreement Services
    • Payment Processing
      • Vendors
      • Patients
  • Study Management
    • Adherence to Good Clinical Practice


SPIRITT TM RESEARCH

12977 North Forty Drive, Suite 200 - St. Louis, MO 63141 USA
Phone 314-738-8026 | FAX 314-548-6221 | jdaegele@spirittresearch.com

©2013-2014 - SPIRITT, LLC