Software

Digital Solutions
for Life Sciences

Technology developed within the Synvia laboratories, with global standards

Our software is born from real-world operations: thousands of clinical studies conducted and millions of laboratory analyses processed. We combine science, technology, and compliance to deliver efficiency, safety, and scalability to the pharmaceutical industry.

Synvia

Synvia TrialCore, the digital core of clinical research

From the eCRF that captures clinical data to the ePRO that collects directly from the participant, through operational management in the CTMS and document governance in the eTMF — everything integrated into a single database, with no silos and no rework.

For those who run highly complex laboratories

Synvia LIS, full automation of the laboratory workflow

From sample collection to result release, Synvia LIS automates the laboratory’s entire workflow, ensuring traceability, efficiency, and compliance proven by international certifications.

Intuitive usability and easy navigation

Intuitive usability and easy navigation

Agility in the release of results

Agility in the release of results

Reduction of errors and rework

Reduction of errors and rework

Secure and traceable operation

Secure and traceable operation

International standards of quality and safety

All of our platforms are developed and validated in compliance with the most rigorous international regulatory standards.

  • FDA 21 CFR Part 11
    FDA 21 CFR Part 11
    FDA 21 CFR Part 11
  • EMA GCP / GLP
    EMA GCP / GLP
    EMA GCP / GLP
  • ANVISA
    ANVISA
    ANVISA
  • ICH
    ICH
    ICH
  • LGPD
    LGPD
    LGPD
  • ISO 17025
    ISO 17025
    ISO 17025
  • CAP
    CAP
    CAP

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.