Automation · Process control · Life Science
Control systems that keep regulated production running.
Uvitech designs, integrates and qualifies automation for Life Science manufacturers: validated server stations for the control layer, and cycle control systems for sterilisation, cleaning and batch processes. Delivered globally, documented to GxP expectations.

Two things we do exceptionally well.
Both are delivered as complete, qualified systems: hardware, software, documentation and on-site commissioning by our own engineers.

Server stations
Engineered server and workstation platforms for SCADA, batch, historian and MES layers. Specified, built, hardened and qualified (IQ/OQ) before they reach your site.
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Cycle control systems
PLC and HMI control for cyclic processes: sterilisation, CIP/SIP, washing, freeze-drying and bioreactor runs. Recipe management, electronic cycle records and full audit trail.
Learn moreHow we work
One team from URS to handover.
A fixed sequence with a named lead engineer throughout. Every step produces a document you can put in front of an auditor.
- 01
Discover & specify
Site walk-through, process review and a User Requirements Specification we write together with your engineering and QA teams.
- 02
Design
Functional and design specifications, network and hardware architecture, risk assessment and a traceability matrix back to the URS.
- 03
Build & test
Panel build, software development and a Factory Acceptance Test at our facility, with your team invited to witness.
- 04
Commission & qualify
Installation, Site Acceptance Test, IQ/OQ execution support, operator training and a documented handover with remote support afterwards.
Global reach
Based in London. Commissioning wherever your plant is.
Our engineers travel to site for FAT, SAT and start-up, and support systems remotely between visits. Documentation is prepared in English as standard.
Home region. Short-notice site visits and same-week engineering support.
Regular projects in pharmaceutical and biotech clusters across the EU and Switzerland.
Delivery for US and Canadian manufacturers, with documentation aligned to FDA expectations.
Greenfield facility projects and equipment upgrades for regional pharmaceutical producers.
Commissioning support for OEM equipment and control system retrofits.
Which control platforms do you work with?
How do you approach computer system validation?
Can you upgrade an existing system without stopping production?
Do you supply hardware or software only?
What does support look like after handover?