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.