Electrical design, PLC, SCADA and robotics under one roof
Industries · Life Sciences & Pharma
Where the record matters as much as the product.
GMP-compliant automation for pharmaceutical production and packaging - with the electronic records, serialisation and audit trail that regulated manufacturing depends on.
The challenge
An unrecorded process is an unprovable process.
In regulated manufacturing, producing the right product is only half the obligation. The other half is being able to demonstrate - months later, to an auditor - exactly how it was produced, by whom, from which materials and under which parameters.
Automation that captures this as a by-product of running the line is far more reliable than a documentation process bolted alongside it.
Our starting point is always the same: instrument the process, agree what good looks like, then automate. Visibility first, optimisation second.
Engineering
Platform
MAPP MES / IIoT for OEE, quality and traceability
Delivery
Virtual commissioning before anything reaches your floor
Support
Global commissioning, with 24/7 remote support for AMC customers
How we help
Capabilities applied to Life Sciences & Pharma.
GMP-compliant automation
Production and packaging automation designed around Good Manufacturing Practice expectations from the first concept sketch.
Electronic batch records
Process parameters, operator actions and material batches recorded automatically against every unit and batch produced.
Audit-ready documentation
FDS, SDS, test scripts and validation-supporting documentation delivered as part of the project, not assembled afterwards.
Serialisation & track and trace
Barcode, QR and RFID identification with full backward and forward traceability across the production lifecycle.
Controlled access & audit trail
Role-based access with version control and complete audit trail across the platform and quality records.
Vision-based verification
Automated verification of labelling, presence, orientation and pack integrity, with the inspection image retained.
Typical applications
Where we are usually asked to help.
- Packaging line automation and integration
- Serialisation and aggregation systems
- Batch parameter recording and electronic records
- Clean-room compatible handling automation
- Label and pack integrity vision inspection
- Utility and environmental condition monitoring
- Validation-supporting documentation packages
- Legacy equipment retrofits with modern records capability
24+
Years of experience
400+
Projects delivered
30+
Countries served
ISO9001
2015 certified
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Most relevant to this sector
Looking for something else?
Get in touch
Automating a regulated line?
Tell us the process and the compliance framework. We will scope automation that produces the record as it produces the product.