Evidence is produced by the work
Method versions, analyst actions, instrument state, approvals and timestamps are recorded as the work happens, not reassembled before an assessment.

Compliance-native LIMS
Synvra is the laboratory information management system for testing and calibration laboratories: one controlled chain from request to certificate, with the evidence recorded as the work happens.

The problem
Results, calibration status, method versions and custody records all exist, in different places, kept by different people and linked by memory. When a customer disputes a result or an assessor asks how it was produced, the answer takes days to reconstruct.
The controlled chain
Request
Customer, order and requested tests, reviewed before work starts.
Receive
Accession, condition checks and chain of custody.
Test
Worksheets bound to an approved method version and a serviceable instrument.
Review
Submission, independent review and release with re-authentication.
Report
A controlled certificate from a versioned template.
Verify
Recipients check it by QR code; withdraw it and the record updates.
Public verification
Every certificate carries a verification reference and a QR code. Your customer, their auditor or a regulator scans it and sees, without an account, whether it is valid or withdrawn. Internal evidence never appears on the public page.
Try it: change the laboratory's record
Valid certificate
Issued by the laboratory and not withdrawn. The details below match the laboratory's record.
Checked against the laboratory's live record, not a copy.
Illustration with demo data from the Synvra demo laboratory.
Why Synvra
Real screens from the product, not mock-ups.
Method versions, analyst actions, instrument state, approvals and timestamps are recorded as the work happens, not reassembled before an assessment.

Results are entered against an approved method version, so the record shows exactly how each one was produced.

Calibration, maintenance and serviceability sit beside the work they support and stay linked to the results they produced.

Results are submitted, reviewed by someone else and released with re-authentication. A rejection goes back to the analyst with the reasons recorded.

Packages
Each package includes the one before it. Add sites and other add-ons as you grow.
Controlled sample-to-report operations, instrument-aware execution and certificates your customers can verify.
What Core includesEverything in Core, plus the quality, competence, metrology and evidence controls that accreditation depends on.
What Compliance includesEverything in Compliance, plus commercial operations and integration for laboratories consolidating several systems.
What Complete includesBuilt for
Accredited and accreditation-seeking third-party laboratories, typically ten to sixty staff on one to several sites. Our focus markets are Pakistan, Saudi Arabia, United Arab Emirates, and we work with laboratories in other countries too.
Residues, contaminants, microbiology and nutrition, with certificates your customers rely on.
Drinking water, wastewater, soil and emissions, with sample custody that holds up.
Reference standards, traceability, uncertainty and decision rules in one place.
Batch and supplier testing with certificates of analysis tied to the evidence.
How you start
A scoping call
Thirty minutes on your workflow, catalogue and accreditation scope.
A 90-day paid pilot
One site, one workflow, your own tests and certificate template.
An annual contract
If it works, the full pilot fee is credited against implementation.
Accountable by design
Thirty minutes on the working product. ISO/IEC 17025-aligned workflow support; accreditation remains the laboratory's responsibility.