Industry

Traceable infrastructure for regulated science

infraOk builds and operates cloud environments for pharma and life-sciences teams that need traceability, controlled change and serious compute, working alongside your quality and validation teams.

Validated and research environments kept apart, with an audit trailA locked, validated environment for regulated systems sits beside a separate research environment with GPU compute. Below them an audit log records each approved change with its author.VALIDATEDRESEARCHCHG-1041 · APPROVED · J.R.CHG-1042 · APPROVED · A.K.
01 / What we hear

What we hear from teams like yours

  • “Every infrastructure change needs a documented impact assessment, and writing it takes longer than the change.”

  • “Researchers want GPUs for protein models; IT wants to know where the data lives.”

  • “A validated system runs on hardware that's out of support.”

  • “An auditor asks who changed a server setting in March, and the answer is in someone's memory.”

02 / Context

What's different about infrastructure for you

In regulated life-sciences work, how a change happens matters as much as the change itself. Systems that touch GxP data need documented configuration, controlled change, access reviews and audit trails that still hold up years later.

Infrastructure as code helps here more than most teams expect. Every change is a reviewed commit with an author and a timestamp, and an environment can be rebuilt exactly. We work alongside your quality and computer system validation teams: they own validation, and we provide the infrastructure documentation, change records and evidence they need.

On the research side, we build compute that scales for genomics pipelines, simulations and AI models, kept apart from validated systems so exploration never puts compliance at risk.

03 / Where we help

Where we help

FAQ

Questions, answered

Does infraOk validate our GxP systems?

No. Validation stays with your quality and computer system validation teams. infraOk provides the infrastructure documentation, change records and configuration evidence they need, in environments designed to support 21 CFR Part 11 and EU GMP Annex 11 requirements.

Can research and regulated workloads share a cloud account?

infraOk usually recommends separate accounts or subscriptions with shared guardrails, so research teams can move quickly without touching the validated environment.

Next step

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