Pharmaceutical & cleanroom.
Our specialism, and the niche we are building toward. Cleanrooms, transfer systems and automated processes under some of the strictest regulatory, cleanliness and validation demands in industry — the projects that are as demanding as engineering gets.
Why these projects are different
Regulatory scrutiny, cleanliness classification, documentation and validation turn an ordinary mechanical problem into a multi-disciplinary one. The equipment has to be serviceable in a space that was never designed to be serviced, and the paperwork has to stand up long after the engineering is finished.
Designed as one system, not four
Mechanical design is developed around the complete system, with process, electrical, automation and software considered from day zero. In a cleanroom that matters more than anywhere else: airflow, material transfer, control philosophy and cleanability all constrain each other, and designing them in sequence is how facilities end up with compromises nobody chose.
Proven before it is built
CFD-validated airflow, FEA on critical structures, 3D scanning of the existing facility and rapid prototypes of the parts we are least certain about. Snags found on screen cost hours; snags found in a live facility cost production.
Retrofit into a running facility
Most of this work goes into buildings that cannot stop. Accurate survey, a realistic plan for the shutdown window, and a plan B for the highest-risk ten per cent — because right on time is what a validated facility actually needs.
Tell us what you're up against.
The earlier we're in, the more paths are still open. Bring us the problem, not a finished specification — we'll tell you what's actually possible and what it will take.