CTMS
Integrated Clinical Trial Management
CTMS
Manage Clinical Trials from Protocol Approval to the Study Closeout through an integrated CTMS on the CARA Life Sciences Platform™. CTMS enables the consistent use of the Study Protocol and Study Master Data along the entire Clinical Trial operations value chain.
Our CTMS provides a single source of truth for all operational Clinical Trial data and workflows. It helps Clinical Trial Managers to make operational decisions based on timely, accurate and consistent data consolidated across simultaneous workstreams like study and site initiation, patient recruitment, monitoring and drug supply.
Benefits
Reach across the organisation
Connect all clinical trial operation workflows through CTMS data & master data
Align disparate workstreams
CTMS on the CARA Life Sciences Platform is the single source of truth for operational data, integrating multiple systems and processes
Adapt to evolving regulations
Conduct clinical trails by adapting the latest regulations to the advantage and safety of enrolled patients
Data Interoperability
The CARA Life Sciences Platform™ with its CTMS supports the industry standard data types and formats for enterprise-wide data exchange.
Collaboration
Clinical Trial end-to-end support
Cara CTMS enables overarching collaboration across sponsor organisations, regulators, sites, investigators, participants, monitors, CRA's, and 3rd parties.
Such collaboration maintains and manages all aspects of Clinical Trials including planning, performance reporting, information sharing, tracking of timelines and milestones across a single platform.
• Clinical Program/Project Management
• Trial and Site planning
• Trial Design
• Site and Subject Management
• Study Management
• Investigator Management
• Clinical Supply Tracking
• Clinical Trial Performance and Reporting
Learn more about RIM
RIM
