CIP and SIP, designed and validated.
We design, build, and qualify clean-in-place and steam-in-place systems, so cleaning and sterilization are validated to EU GMP Annex 1 before production starts.
From layout to a qualified cycle.
CIP and SIP succeed or fail on the details that are hardest to see once the equipment is installed. We get them right before they are built in.
System design review, slope and drainability, and vendor challenge before procurement, so the design is right before anything is ordered.
We find and design out dead legs and unswept volumes that quietly fail cleaning and sterilization.
CIP spray coverage and riboflavin testing, SIP temperature mapping, condensate removal, and air removal verified.
Full qualification with audit-ready documentation, built to EU GMP Annex 1 and SFDA-aligned for the Gulf.
Validated before the walls go up.
We have run CIP/SIP layout validation and vendor challenge inside sterile facilities still under construction, aligning the design and eliminating dead legs before procurement rather than discovering them at qualification.
Why it matters. A dead leg or a poorly drained line found at PQ is expensive and late. Found at design review, it is a markup. We bring the second set of eyes that catches it early.
Common questions.
System layout, slope and drainability, spray coverage, dead-leg review, and a vendor challenge of the proposed design, ideally before procurement.
We identify dead legs and unswept volumes in the design and redesign them out, then verify cleaning and sterilization reach every surface.
EU GMP Annex 1, with SFDA alignment for Gulf projects, through IQ, OQ, and PQ.
A named senior specialist with a published CV, embedded in your team from day one.
Fixed-price milestones with GMP-compliant deliverables and a conceptual brief before you commit.
Send us your CIP/SIP scope and timeline. We reply with a conceptual brief and next steps.