Paul Industries delivers CIP/SIP systems for biotech & bioprocessing as a single-source supplier and installer. We design, fabricate, install, passivate, and validate CIP/SIP systems – the clean-in-place and steam-in-place circuits that sterilize and clean a process train without disassembly – built to the standards your process and your auditors require.
What biotech & bioprocessing need from cip/sip systems
Bioprocessing adds a layer of complexity beyond traditional pharma: living cell cultures, single-use and stainless hybrid trains, bioreactors, and aseptic fill-finish. Cell and gene therapy suites push classification and segregation even harder. The water, piping, and cleanroom systems supporting biologics have to protect sterility and product integrity at every step.
For this work, that means aseptic processing, single-use/stainless integration, WFI and clean steam for bioreactors, and Grade A/B cleanroom segregation – not as an afterthought, but engineered in from the first drawing.
What we deliver
- Clean-in-place (CIP) skids – single-use or recirculating, with spray-device coverage engineered for full wetted-surface contact
- Steam-in-place (SIP) circuits designed for condensate removal, sterilization hold, and validated F0 delivery
- Integration with your process piping so CIP/SIP loops actually reach every dead-leg and instrument
- Cycle development and documentation to support cleaning and sterilization validation
- Controls and recipe management for repeatable, auditable cycles
One accountable partner
Most biotech projects get split between an equipment supplier and an install contractor – and the validation burden falls in the gap between them. Paul Industries closes that gap by self-performing the whole scope, from supply through documented turnover.
Related: CIP/SIP Systems services · Biotech & Bioprocessing solutions · Request a quote
Frequently asked questions
What biotech requirements do you build to?
Our cip/sip systems work for biotech & bioprocessing is built around aseptic processing, single-use/stainless integration, WFI and clean steam for bioreactors, and Grade A/B cleanroom segregation. Every installation ships with the documentation your quality team needs.
Do you handle validation, or just installation?
Both. We install and then support IQ/OQ/PQ with turnover packages, weld/material traceability, and test records – so the system is not just built, it is provable.
Can you take a project from design through startup?
Yes – that is the point of single-source. Design, fabrication, installation, passivation, and commissioning for your biotech process, under one accountable partner.
Get a single-source quote
Paul Industries designs, fabricates, installs, passivates, and validates – one accountable partner instead of a vendor plus a contractor plus a validation firm. Tell us about your project and we will scope it.