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Custom software for laboratories and biotechnology

From samples to results, laboratories need to track data, processing stages and approvals. Saviano develops business applications for biology and biotechnology teams around their instruments, existing software and validation responsibilities.

Organise sample and result workflows

Together with your team, we map receipt, identification, processing, checks and approval. Statuses, roles and the information to retain are defined before development starts.

A portal can centralise requests and progress tracking, while technician views support data entry and checks. Identifiers and event history should let authorised users trace each result back to its source and the actions performed.

Connect instrument data to business tools

Imports use file formats or interfaces actually available on your instruments. We define field mapping, format validation and error handling before implementing exchanges.

The project can complement an existing LIMS or ELN rather than replace it. The selected functions depend on your interfaces, business rules and the scope the team actually needs.

Keep human approval and plan ongoing maintenance

Automation prepares data and flags inconsistencies; authorised people retain responsibility for business decisions. Permissions, logs and approval stages are checked using representative scenarios.

Regulatory requirements, qualification and any clinical obligations must be identified with the responsible specialists. The project specifies the evidence and responsibilities required; software development does not itself constitute clinical certification.

Illustrative applications

Illustrative application: sample tracking and result imports

These scenarios illustrate possible applications. They are not client case studies or reported project results.

A portal tracks samples, imports instrument files and flags inconsistent data. An authorised user reviews and approves results before release. This is a possible scenario rather than a named client case.

Frequent questions

Custom software for laboratories and biotechnology

Do we need to replace our LIMS or ELN?

Not necessarily. An application can cover a specific workflow and exchange information with your existing tools where their interfaces and access conditions allow it.

Can instrument imports be automated?

We first verify the available interfaces and formats. Imports are then tested with representative files, known errors and the agreed consistency checks.

How are validation obligations defined?

Your business and regulatory leads identify the applicable requirements. Scoping defines functions, tests, documentation and the person responsible for each approval.

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