VirTrial
Signant Health is a global provider of clinical trial technologies and services, dedicated to generating high-quality trial data. With over 30 years of experience, they support thousands of trials and have contributed to hundreds of drug approvals. Their mission is to deliver reliable, high-quality data through comprehensive eClinical solutions, simplifying patient and site participation, managing global IP supply chains, and providing in-study analytics. They operate offices worldwide, offering tailored support with a deep understanding of local regulations and cultural nuances, and also provide flexible remote work options.
Industries
Nr. of Employees
small (1-50)
VirTrial
785 Arbor Way, Blue Bell, PA 19422
Products
eCOA / ePRO platform
Software platform for electronic capture of patient-reported outcomes and eDiaries with language management, scale management and BYOD support.
Electronic data capture (EDC) platform
EDC system for collecting and managing clinical trial data with options for self-service study build and integration with other eClinical modules.
Unified eClinical platform
Integrated platform combining EDC, eCOA, RTSM and analytics modules to provide an end-to-end study management environment.
RTSM and study supply management system
System for randomization, trial supply management and cohort-specific drug dispensation with support for direct-to-patient and complex dosing strategies.
Clinical supply chain and GxP inventory software
Cloud-based tools for managing GxP inventory, forecasting, lot recall and integrations with labeling systems.
Clinical Data Hub and Data Workbench
Centralized data repository and workbench tools for data review, aggregation and study oversight, enabling RBQM and analytics workflows.
eCOA / ePRO platform
Software platform for electronic capture of patient-reported outcomes and eDiaries with language management, scale management and BYOD support.
Electronic data capture (EDC) platform
EDC system for collecting and managing clinical trial data with options for self-service study build and integration with other eClinical modules.
Unified eClinical platform
Integrated platform combining EDC, eCOA, RTSM and analytics modules to provide an end-to-end study management environment.
RTSM and study supply management system
System for randomization, trial supply management and cohort-specific drug dispensation with support for direct-to-patient and complex dosing strategies.
Clinical supply chain and GxP inventory software
Cloud-based tools for managing GxP inventory, forecasting, lot recall and integrations with labeling systems.
Clinical Data Hub and Data Workbench
Centralized data repository and workbench tools for data review, aggregation and study oversight, enabling RBQM and analytics workflows.
Services
Early-stage protocol guidance and COA measurement strategy provided by in-house clinicians and scientists to inform endpoint selection and assessment design.
Operational implementation, study build and project management for EDC/eCOA/RTSM studies, including options for accelerated or self-service builds and local/global deployment support.
Provision of blinded analytics and central review to detect rater/site anomalies, validate inclusion criteria, detect fraudulent patterns and support go/no-go decisions.
Rater training programs, qualification and calibration services to improve consistency in clinician-administered assessments and support centralized rating processes.
Forecasting, planning and inventory management services for GxP supplies, including integration with supply chain software and processes for lot recall and direct-to-patient models.
API integration support, marketplace connectivity and single sign-on/identity portal implementations to connect third-party systems with the core eClinical platform.
Early-stage protocol guidance and COA measurement strategy provided by in-house clinicians and scientists to inform endpoint selection and assessment design.
Operational implementation, study build and project management for EDC/eCOA/RTSM studies, including options for accelerated or self-service builds and local/global deployment support.
Provision of blinded analytics and central review to detect rater/site anomalies, validate inclusion criteria, detect fraudulent patterns and support go/no-go decisions.
Rater training programs, qualification and calibration services to improve consistency in clinician-administered assessments and support centralized rating processes.
Forecasting, planning and inventory management services for GxP supplies, including integration with supply chain software and processes for lot recall and direct-to-patient models.
API integration support, marketplace connectivity and single sign-on/identity portal implementations to connect third-party systems with the core eClinical platform.
Expertise Areas
- Clinical trial management and site oversight
- eCOA and patient-reported outcomes (PRO) capture
- Electronic data capture (EDC) and clinical data management
- Randomization and trial supply management (RTSM)
Key Technologies
- eCOA / ePRO capture
- Electronic data capture (EDC)
- Unified eClinical platform
- Randomization and trial supply management (RTSM)
News & Updates
A case study on how Signant's solutions helped accelerate COVID-19 trials in Japan.
A case study on how PureSignal Analytics improves assessment quality in schizophrenia trials.
A testimonial on how UNBOUND saved time and increased project speed.
A case study on how Signant's solutions helped accelerate COVID-19 trials in Japan.
A case study on how PureSignal Analytics improves assessment quality in schizophrenia trials.
A testimonial on how UNBOUND saved time and increased project speed.