
Synvia CTMS: Complete operational management of the clinical study

The central platform for operational management of clinical trials.
As part of the Synvia Trial Core ecosystem, Synvia CTMS centralizes and governs the clinical operation with data, control, and performance throughout the entire study.
Full visibility of the study portfolio
Centralize data, processes, and indicators in a single environment.
Full visibility of the study portfolio
Centralize data, processes, and indicators in a single environment.
Faster, more predictable, and controlled trials
Identify, record, and proactively manage corrective actions.
Faster, more predictable, and controlled trials
Identify, record, and proactively manage corrective actions.
Data-driven decision making based on updated information
Interactive dashboards and updated reports for quick and well-informed strategies
Data-driven decision making based on updated information
Interactive dashboards and updated reports for quick and well-informed strategies
Proactive reduction of operational risks and deviations
Sponsors, CROs, and research centers working from the same reliable source of information
Proactive reduction of operational risks and deviations
Sponsors, CROs, and research centers working from the same reliable source of information
Full visibility of the study portfolio
Centralize data, processes, and indicators in a single environment.
Data-driven decision making based on updated information
Interactive dashboards and updated reports for quick and well-informed strategies
Faster, more predictable, and controlled trials
Identify, record, and proactively manage corrective actions.
Proactive reduction of operational risks and deviations
Sponsors, CROs, and research centers working from the same reliable source of information
Main modules
Study management
Definition of milestones and activities with assignment of responsibilities
Research centers
Registration, activation, and continuous monitoring of performance and quality
Clinical monitoring
Standardized management of visits, reports, and findings
Recruitment
Screening, inclusion, and randomization versus real-time study goals
Financial management
Specific and detailed reports available in real time for monitoring and management.
Integration
Native connection with other Synvia clinical solutions
Study management
Definition of milestones and activities with assignment of responsibilities
Clinical monitoring
Standardized management of visits, reports, and findings
Financial management
Specific and detailed reports available in real time for monitoring and management.
Research centers
Registration, activation, and continuous monitoring of performance and quality
Recruitment
Screening, inclusion, and randomization versus real-time study goals
Integration
Native connection with other Synvia clinical solutions
Integration
Native connection with other Synvia clinical solutions
Financial management
Detailed reports available in real time for monitoring and management
Recruitment
Screening, inclusion, and randomization versus real-time study goals
Clinical monitoring
Standardized management of visits, reports, and findings
Research centers
Registration, activation, and continuous monitoring of performance and quality
Study management
Definition of milestones and activities with assignment of responsibilities
Integration
Native connection with other Synvia clinical solutions
Financial management
Detailed reports available in real time for monitoring and management
Recruitment
Screening, inclusion, and randomization versus real-time study goals
Clinical monitoring
Standardized management of visits, reports, and findings
Research centers
Registration, activation, and continuous monitoring of performance and quality
Study management
Definition of milestones and activities with assignment of responsibilities
Other TrialCore solutions: The digital core of clinical research
Other TrialCore solutions: The digital core of clinical research
An integrated ecosystem of software that organizes, connects, and scales clinical operations, from planning to the completion of the study.
Synvia eCRF
Electronic data capture (EDC) platform with security, audit trails, and FDA 21 CFR Part 11 compliance.
Synvia eCRF
Electronic data capture (EDC) platform with security, audit trails, and FDA 21 CFR Part 11 compliance.
Synvia eTMF
Electronic Trial Master File management platform with organization, traceability, and version control of regulatory documents.
Synvia eTMF
Electronic Trial Master File management platform with organization, traceability, and version control of regulatory documents.
Synvia ePRO
Platform for structured collection of participant-reported data via mobile app.
Synvia ePRO
Platform for structured collection of participant-reported data via mobile app.
ASynvia
Technology developed within the Synvia laboratories, with global standards.
Created by those who live the practice of research and laboratory, our software combines science, technology, and compliance to deliver efficiency, safety, and scalability to the operations of the pharmaceutical industry.

Contact
Talk to our experts
Discover how Synvia can support your studies, analyses, and projects.

Contact
Talk to our experts
Discover how Synvia can support your studies, analyses, and projects.

