Custom automation engineered for cleanrooms, where every square foot is a line item and every component has to earn its place. Built for life sciences and pharmaceutical manufacturers near the Boston Biohub and beyond.
In a cleanroom priced at around one thousand dollars per square foot, automation has to do more with less. Less floor space. Less maintenance access. Fewer components to validate. Less tolerance for anything non-essential. We design cleanroom automation around those constraints from the start, so the machinery fits the room, not the other way around.
Purpose-built components let us deliver complex processes in tight footprints. The same capability, in a fraction of the floor space standard equipment would demand.
Our cleanroom equipment starts with welded-steel frames that won’t misalign over time. Critical for validated environments, where equipment drift costs you more than downtime.
Surfaces, materials, and construction specified for controlled environments. Built to meet the cleanliness, chemical compatibility, and documentation requirements your process demands.
Custom software built in-house, designed for cleanroom operations. Recipe handling, validated data logging, and integration with your existing SCADA or MES platforms.
Equipment documented and built to support your IQ, OQ, and PQ protocols. We work alongside your validation team from design through commissioning.
Our shop in Keene, New Hampshire, sits within close reach of the Boston Biohub, the densest concentration of life science and pharma manufacturing in the country. That proximity means shorter design cycles, faster response times, and engineers who can be in your facility when a project needs hands-on collaboration.
Few custom automation partners can match it.
We start by learning your cleanroom specs, the process you’re automating, the validation path you have to follow, and the footprint you have to fit.
Our engineers design the system around your cleanroom classification, floor space, and integration requirements. Then we refine it with your team.
Through ProTwin MCS, the full system is tested in a virtual environment before fabrication. Control logic, operator flow, and clearance issues surface in software, not after installation.
In-house fabrication and assembly, followed by factory acceptance testing and coordinated support for your validation protocols on-site.
Automation for research, diagnostic, and medical device manufacturing environments where cleanliness, footprint, and documentation all matter at once.
Cleanroom-ready equipment for drug production, fill and finish, and packaging environments built to validated production standards.
Custom automation for cell and gene therapy, bioprocessing, and emerging therapeutic manufacturing, where process flexibility is as critical as compliance.
Custom production machinery, often the core of a larger integration project.
Automated test stations and inspection systems are engineered for controlled environments when required.
SCADA, HMI, and data systems built to support validated environments.