ClinicalPURSUIT
ClinicalPURSUIT is a division of Global Vision Technologies, Inc., specializing in powerful clinical trial data management solutions, including electronic data capture (EDC) software, patient registry software, and related services. The company aims to streamline clinical trials, improve data quality, and accelerate research through innovative technology and user-friendly systems. It emphasizes rapid deployment, intelligent data capture, and intuitive dashboards in its EDC systems, and offers solutions tailored to various study types with strong technical support. The company also provides comprehensive solutions for remote monitoring, data validation, and trial management, ensuring compliance with regulatory standards and enhancing data quality and study efficiency.
Industries
Nr. of Employees
small (1-50)
ClinicalPURSUIT
Products
Centralized clinical data management platform
A centralized clinical data platform for enrollment, eConsent, eCRF capture, validation, query management, randomization integration and reporting for multi-site studies.
Centralized clinical data management platform
A centralized clinical data platform for enrollment, eConsent, eCRF capture, validation, query management, randomization integration and reporting for multi-site studies.
Services
EDC study implementation and configuration
Study configuration, CRF design, QA and deployment services to implement validated electronic data capture studies aligned to protocol and regulatory data standards.
Randomization and trial supply management services
Design and integration of randomization schedules, stratified allocations, supply inventory controls, automated reordering and product history/traceability integrated with trial data systems.
Patient registry design and deployment
Creation and hosting of centralized registries for longitudinal patient data capture, benchmarking and outcome monitoring across sites.
Implementation support, training and validation assistance
Live demonstrations, onboarding training, technical support and guidance for system validation and user acceptance testing.
EDC study implementation and configuration
Study configuration, CRF design, QA and deployment services to implement validated electronic data capture studies aligned to protocol and regulatory data standards.
Randomization and trial supply management services
Design and integration of randomization schedules, stratified allocations, supply inventory controls, automated reordering and product history/traceability integrated with trial data systems.
Patient registry design and deployment
Creation and hosting of centralized registries for longitudinal patient data capture, benchmarking and outcome monitoring across sites.
Implementation support, training and validation assistance
Live demonstrations, onboarding training, technical support and guidance for system validation and user acceptance testing.
Expertise Areas
- Clinical trial data management
- Electronic data capture (EDC) implementation and validation
- Randomization and trial supply management (RTSM)
- Electronic patient-reported outcomes (ePRO/eCOA)
Key Technologies
- Electronic data capture (EDC) platforms
- ePRO / eCOA capture
- Randomization and trial supply management (RTSM)
- Clinical trial management system (CTMS) integration