Sterile environments built to spec — and built to hold spec.
Veridian Process Group designs and builds ISO-classified clean rooms for peptide compounding — from ground-up construction to modifying and expanding the facility you already have.
Building a clean room from an empty room or a raw shell.
For pharmacies and labs standing up peptide compounding capability for the first time, or replacing a facility that's reached its limit.
- ISO classification design matched to your compounding volume and USP <797>/<800> scope
- Modular wall, ceiling grid, and epoxy flooring systems
- HVAC, HEPA filtration, and pressure cascade engineering
- Pass-throughs, gowning rooms, and sink placement to match workflow
- Certification, particle counts, and documentation for state board inspection
Upgrading, requalifying, or growing the room you already run.
For facilities adding volume, adding a hazardous compounding line, or bringing an aging room back up to current classification.
- Facility assessment against current ISO 14644-1 and USP requirements
- Phased construction that keeps existing operations running
- Added anterooms, negative-pressure suites, or a second PEC line
- HVAC rebalancing and filter upgrades without a full teardown
- Re-certification and updated documentation on completion
Site Assessment & Classification Design
We walk the space, review your compounding volume, and set the ISO classes and room adjacencies the layout needs to hit.
Architectural & MEP Engineering
Wall, ceiling, airflow, and pressure cascade drawings — built to route around your existing structure, not fight it.
Construction
Modular panel systems, epoxy or welded vinyl flooring, gowning rooms, and pass-throughs installed with minimal site disruption.
Certification & Commissioning
Particle counts, smoke studies, and pressure verification, with the documentation package your inspector will ask for.
We design and build to the standards above and coordinate documentation for your inspection. Final certification is issued by your accredited third-party certifier and your facility's compliance remains the responsibility of its licensed pharmacist-in-charge.
503B Outsourcing Facility — Ground-Up Build
A 2,400 sq. ft. peptide compounding suite built from a raw warehouse shell, including gowning, buffer, and a two-hood PEC line.
Hospital Compounding Pharmacy — Full Retrofit
Reclassified an aging USP <795> room to current <797> standard in phases, without closing the pharmacy.
Biotech Peptide R&D Lab — Expansion
Added a second ISO 7 suite and negative-pressure anteroom to an existing clean room to double compounding capacity.
Veridian Process Group was the only contractor who asked about our actual workflow before drawing anything. The room they built is the first one our inspector didn't flag a single note on.
Tell us the room you have — or the one you're planning.
Every project starts with a site visit or a set of your existing drawings. From there we scope classification, timeline, and cost before any construction begins.