Data Management
We know at the end of a trial, the success you achieve is based on the quality of your data. From protocol development and CRF design through CRF completion instructions and site training, our data management group pulls together all aspects of the trial to promote data integrity. NaviGo has the resources and expertise to provide everything from guidance and support for your in-house team to being a full service data management resource capable of completing the entire project for you.
Key Data Management services include:
- Case Report Form (CRF) design and development
- Database design, build, validation and management
- Data entry and processing
- Query development, tracking and resolution
- Paper and Electronic Data Capture (EDC)
- On-site support and hosting services
- Clinical Trial Management Tools (CTMS)
- Study document tracking
- eMonitoring
- IRB/EC Submission Tracking
- Data review
- Adverse Event (AE) tracking and reporting
- AE preparation for DSMB
- Development of Site Payment Rules
- Monitoring Setup
- Automated notifications from database
- Protocol and IRB submission Tracking
- Site Tracking
- Customized Report Creation and Development
- Data Export capability and interface with multiple file formats (i.e. SAS)
- Secure Storage for paper based trials
- Trial Support/Helpline
- Training documents and support
