Laboratory
Data Migration

Move legacy lab data without losing the structure, lineage, and auditability your teams depend on.

THE CHALLENGE

Moving legacy data is easy. Preserving what it means is harder.

Formats, relationships, history, and audit trails can break when legacy records move without careful mapping and validation.

01

Lost context

Critical context and history can disappear between systems.

02

Broken lineage

Links between samples, results, and records can break.

03

Validation debt

Missing checks and documentation delay trust in the new system.

04

Operational disruption

Poor migration planning slows teams and puts ongoing work at risk.

DATA INTEGRITY

From legacy records to trusted, traceable data

Map, validate, and reconcile fragmented records into one clean, audit-ready platform.

Validation LayerLEGACY SOURCESSpreadsheetsSQL recordsLegacy LIMSPaper logsUNIFIED PLATFORMUnified recordsData modelAudit trailReports

Segments we serve

Across the biotech
& life sciences ecosystem

CRO

Run more studies across clients without multiplying manual coordination.

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Our process

How We Migrate
Laboratory Data

A structured process for moving lab data safely, preserving integrity and traceability, and keeping systems reliable through cutover.

01. Assessment

We assess your source systems and data landscape.

We review existing records, formats, and system dependencies before planning the migration.

  • Source system review
  • Data volume analysis
  • Dependency mapping
RecordsFormatsVolumeSystemsDependenciesRisks

segments we serve

Across the biotech
ecosystem

Deep Biotech Expertise

Deep Biotech Expertise

Less time explaining how scientific work operates. More time solving the right problem.

Operational Scalability

Operational Scalability

Systems designed to support growth without multiplying manual coordination.

Workflow-Centered Design

Workflow-Centered Design

Built around real laboratory work, not generic software assumptions.

Compliance-Ready Architecture

Compliance-Ready Architecture

Traceability, validation, and audit readiness built in from the start.

GDPR, HIPAA
21 CFR Part 11, GxP & GAMP 5

Experience with regulated systems. Software architecture and development practices designed around the requirements of GDPR, HIPAA, 21 CFR Part 11 and GxP / GAMP 5.

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