Synvia eTMF

Synvia eTMF:
Continuous readiness for inspections

Synvia eTMF: continuous readiness for inspections

Document governance,
with control and visibility.

The digital platform that centralizes essential documents of your clinical study, ensuring governance, traceability, and regulatory compliance.

Clinical operations on a platform

Single repository to manage all study documents

Clinical operations on a platform

Single repository to manage all study documents

Quick and intuitive settings

Creation of records, data entry, access, and simplified settings

Quick and intuitive settings

Creation of records, data entry, access, and simplified settings

Reduction of operational risks

Review, approval and quality flows, with complete audit trails

Reduction of operational risks

Review, approval and quality flows, with complete audit trails

Clinical operations on a platform

Single repository to manage all study documents

Quick and intuitive settings

Creation of records, data entry, access, and simplified settings

Reduction of operational risks

Review, approval and quality flows, with complete audit trails

Integrated and agile collaboration among all involved

Greater efficiency in the collaborative work between sponsors, CROs, and research centers

Integrated and agile collaboration among all involved

Greater efficiency in the collaborative work between sponsors, CROs, and research centers

Integrity, traceability, and versioning of documents

Version control and change history

Integrity, traceability, and versioning of documents

Version control and change history

Synvia eTMF integrates document governance with clinical operations, featuring structured and traceable management.

Synvia eTMF integrates document governance with clinical operations, featuring structured and traceable management.

Standardized structures and expected document lists (EDLs)

Standardized structures and expected document lists (EDLs)

Data protection and robust access management, with folder permissions

Data protection and robust access management, with folder permissions

Simplification of TMF activities, with a real-time view of the status

Simplification of TMF activities, with a real-time view of the status

Detailed and auditable record of all actions in the system

Detailed and auditable record of all actions in the system

Structured transfer of the TMF at the end of the study

Structured transfer of the TMF at the end of the study

Integration with other Synvia clinical systems

Integration with other Synvia clinical systems

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 clinical data capture (EDC) platform with security, audit trails, and FDA 21 CFR Part 11 compliance.

Synvia eCRF

Electronic clinical data capture (EDC) platform with security, audit trails, and FDA 21 CFR Part 11 compliance.

Synvia CTMS

Operational management platform for clinical studies, with milestone tracking, monitoring, recruitment, and financial management.

Synvia CTMS

Operational management platform for clinical studies, with milestone tracking, monitoring, recruitment, and financial management.

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.

Synvia

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.