Single-source process-equipment & sanitary-piping contractor
Paul Industries designs, fabricates, installs, and validates process systems and sanitary piping for pharmaceutical, biotech, cosmetic, nutraceutical, and food & beverage manufacturing facilities across the United States — 30+ years, cGMP/FDA-compliant, delivered under one accountable contract.
Frequently asked questions
What does Paul Industries actually do?
Paul Industries is a single-source process-equipment and sanitary-piping contractor. We design, fabricate, install, passivate and support the qualification of high-purity water systems, sanitary process piping, cleanrooms, CIP and SIP systems and turnkey process systems for regulated manufacturing across the United States.
What does single-source mean in practice?
It means one party is accountable for engineering, fabrication, installation and validation support, so there is no gap between an equipment supplier, an installer and a validation contractor. That gap, rather than any individual scope, is where most process projects lose time and money.
Which industries does Paul Industries serve?
Pharmaceutical, biotech, sterile injectables, medical device, high-containment and antibody-drug conjugate work, nutraceutical, cosmetic, food and beverage, dairy, meat and poultry, distilling and brewing, and cannabis extraction. The engineering overlaps. The regulatory framework each one is inspected against does not.
Where does Paul Industries work?
All 50 US states. Crews mobilise to the site, and shop fabrication is used wherever it reduces field time, which is what makes nationwide coverage practical for specialised sanitary work.
What standards does Paul Industries build to?
ASME B31.3 for pressure piping, ASME BPE for hygienic product-contact systems, ASTM A967 and A380 for passivation and cleaning, ISO 14644 for cleanrooms, and the cGMP framework under 21 CFR that the facility is inspected against.
Does Paul Industries handle validation as well as installation?
Yes. Installation, operational and performance qualification support is scoped alongside the build so the evidence is produced as the work proceeds rather than reconstructed afterwards. Reconstruction is where schedules fail.
Can Paul Industries work in an operating facility?
Yes, and most projects are in live plants. Work is planned against production and sanitation windows, with isolation, defined material routes and each shift ending with the plant able to run.
Does Paul Industries service systems it did not build?
Yes, including maintenance contracts, passivation, derouging, remediation and emergency repair on systems installed by others. The first step is a condition and documentation survey rather than an assumption that the drawings are current.
How long has Paul Industries been doing this?
More than 30 years of cGMP and FDA-compliant process work, self-performing the engineering, fabrication, orbital-welded installation and qualification support rather than subcontracting the specialised scope.
How does a project with Paul Industries start?
With a conversation about the facility, the systems and the timeline, usually followed by a site visit where the work is in an existing plant. Tie-in conditions and access drive the cost more than the drawings do.
