IT for pharma and life science: data that stands the test of time
You work under strict requirements for data security, traceability and controlled operations. We build your IT so you can document it, today and in five years.
Everyday life under regulation
Traceability is a requirement. Every change, every access and every restore must be documented, also five years from now.
In pharma and life science, IT is part of the quality system, not just a work tool. The documentation has to hold up, also when an auditor comes knocking several years later.
You get IT operations built for regulated environments from the ground up. That means controlled access, documented changes, tested recovery and an incident response plan for critical incidents. We take responsibility for operations, so it holds up over time.
The result: you can answer an auditor without a frantic scramble. Your data is protected at a level that matches the industry's requirements, and the quality team can document the IT side of the quality system without friction.
Six things you gain. For quality, operations and documentation.
From audit to validation: here is what the agreement means for the quality team and for operations.
Audit-ready documentation every day
Logging, change management and access history are in place and can be retrieved in one search, not an archive hunt.
Controlled access at every level
Only the right staff see the right data. Changes to access rights are documented and can be rolled back.
Restore is tested, not hoped for
Restores are tested regularly, so you never discover during an incident that the backup couldn't be read back.
Stable operations in critical windows
Preventive monitoring catches problems before they hit production, the lab or quality work.
An incident response plan you can activate today
When something goes wrong, you know who does what in the first 30 minutes, without collecting phone numbers in a panic.
Validated environments that stay put
Changes are controlled, documented and released in a managed way. Your validation is not invalidated by an unannounced patch.
How we work together
Operations built for the quality system. A review of the environment, then a plan with change control, documented operations and tested recovery.
The first step is a review of your environment, where we map the IT elements that are part of the quality system. Then we put together a plan with change control, documented operations and tested recovery. You get named contacts and a service agreement that respects that your time goes to quality work, not IT faults.
No-obligation first conversation
Let's talk about your regulated IT
30 minutes: we listen, point out the three most important improvements and send you a proposal. No sales pitch, no obligation.
IT that stands the test of time. Tell us what matters most, and get a reply, typically the same day on weekdays.
You get a review of your setup and a concrete plan for traceable, controlled operations.