Education and Training


  • Infrastructure and Resource Support for Evidence Collection

  • Good Clinical Practice Training

  • Tips for Publishing Patient Reported Outcome Data

  • Best Practice for Subject Recruitment

  • Best Practice for Subject Retention and Compliance

  • Protocol Development

  • Institutional Review Board Processes

  • U.S. Regulation Training for Biologics, Investigational New Drugs, and Investigational Device Exemptions

  • Provide Research Responsibility Training for the Following Roles:
    • Principal Investigators
    • Sub-Investigators
    • Study Coordinators
    • Trial Managers
    • Administrative Assistants
    • Recruitment Specialists
    • Regulatory Associates/Coordinators
    • Site Managers
    • Clinical Research Associates/Monitors



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

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