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
- Study Management
- Adherence to Good Clinical Practice