clinCORE’s Clinical Trial Management System is a tool for managing every stage of the clinical trial life cycle from start-up to close-out. We have developed powerful tools for managing data through every stage of the clinical trial life cycle.
Our Clinical Trial Management System (CTMS) can accomplish the following and more:
Clinical Study Initiation
- Study identification
- Proposal development
- Confidentiality Agreement (CDA)
- Coverage Analysis
- Budget
- Ancillary services
- Time and effort planning
- Budget negotiations with sponsor
- Clinical Trial Agreement (CTA)
- Institutional Review Board Coordination (IRB)
- Study account(s) creation and setup
- Sponsor invoicing
- Regulatory Documents
- Study activation
Clinical Study Management
- Informed consent
- Subject recruitment
- Subject enrollment
- Subject scheduling
- Data management
- Case report form (CRF)
- Reportable events
- Significant new information/findings (SNIF)
- Protocol amendments
- Study reporting
- Audit and Monitoring
Finance Management
- Effort tracking
- Clinical trials billing
- Charge Master
- Research Orders
- Charge reconciliation
- Charge capture/entry
- Sponsor invoicing and A/R management
Clinical Study Close-out
- Initiate study close out
- Account reconciliation
- Inactivate award account(s) in financial system
- Maintain and submit technical reports to sponsor
- Post-trial Audit / monitoring