Software

Synvia LIS

Synvia LIS: efficiency, safety, and results

Quality and safety

Intelligent management for laboratories that require precision

The Synvia LIS automates the complete workflow of the laboratory — from sample collection to result release — ensuring traceability, efficiency, and proven compliance recognized by international certifications.

CAP
CAP
CAP
ISO 17025
ISO 17025
ISO 17025

Born at the bench, designed for operations

Scientific Authority

20 years operating laboratories under international standards

Scientific Authority

20 years operating laboratories under international standards

Native Interoperability

Ready-made connectors for health plans (FHIR, HL7, TISS)

Native Interoperability

Ready-made connectors for health plans (FHIR, HL7, TISS)

Agile Deployment

Expert-driven configuration

Agile Deployment

Expert-driven configuration

Operation-Centered Design

Modern interface focused on daily lab operations

Operation-Centered Design

Modern interface focused on daily lab operations

National platform, global standard

National platform,
global standard

Modern usability and intuitive experience

Modern usability and intuitive experience

Performance and compliance

Performance and compliance

Personalized, responsive, and specialized support

Personalized, responsive, and specialized support

Agility in the release of results

Agility in the release of results

Reduction of errors and rework

Reduction of errors and rework

Secure, traceable, and scalable operation

Secure, traceable, and scalable operation

For whom

Made for laboratories that want to grow with high productivity and efficiency

Scalable, lightweight, and interoperable, the Synvia LIS supports both small laboratories and large operations with multiple units and processing areas, maintaining standardization, traceability, and performance.

Other TrialCore solutions: The digital core of clinical research

Other TrialCore solutions: The digital core of clinical research

Other digital solutions

CTOX

Digital platform for toxicological test management

CTOX

Digital platform for toxicological test management

Synvia BIO

Comprehensive management of bioequivalence and pharmacological equivalence studies

Synvia BIO

Comprehensive management of bioequivalence and pharmacological equivalence studies

Synvia eCRF

Electronic data capture platform for clinical data with FDA 21 CFR Part 11 compliance

Synvia eCRF

Electronic data capture platform for clinical data with FDA 21 CFR Part 11 compliance

More than software: operation, science, and compliance in the same DNA

Synvia LIS is born within a real ecosystem of certified laboratories that have been serving the Pharmaceutical Industry for 20 years. This means less risk, rapid implementation, and total regulatory compliance.

+800

+800

employees

employees

+3 k

+3 k

partner laboratories

laboratories

partners

laboratories

partners

+200

+200

global customers

clients

global

clients

global

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.