Turnkey MEP and validation for cleanroom facilities.
Mechanical, electrical and plumbing executed as one coordinated scope, and closed out with the qualification documentation that makes the facility usable.
Three services, one coordination model
MEP failures are almost always coordination failures: a duct routed through a cable tray, a drain that cannot fall, a panel that will not fit the room left for it. Holding all three disciplines in one scope is how those get resolved on a drawing rather than on site.
Mechanical
- Air handling units & dehumidification
- Chillers and chilled-water piping
- GI / Aluminium / SS ducting
- HEPA terminal filtration
- VFD and control integration
Electrical
- HVAC power panels & MCC
- Control panels & PLC systems
- GMP light fixtures
- Cleanroom wiring & sockets
- Earthing & safety systems
Plumbing & Utilities
- Chilled and hot water piping
- Drain and condensate lines
- Insulated utility piping
- Pump house & cooling towers
- Compressed air distribution
A facility is not finished until it is documented.
cGMP validation is not a phase bolted on at the end. Protocols and acceptance criteria are agreed before fabrication begins, so qualification confirms the design rather than repairing it.
Design Qualification
Your User Requirement Specification translated into an approved design basis covering classification per room, pressure cascade, setpoints and tolerances, all documented and signed before engineering starts.
Installation Qualification
Documented verification that everything installed matches the approved design: equipment identity, materials of construction, drawings as-built, calibration records and utility connections.
Operational Qualification
Demonstration that the facility performs to the design basis, measuring air changes, particle counts, pressure differentials, temperature and RH, filter integrity, and recovery time against acceptance criteria.
What the dossier contains
- DQ, IQ and OQ protocols and executed reports
- Factory acceptance test (FAT) and site acceptance test (SAT) records
- Material and test certificates for panels, ducting and equipment
- Calibration certificates for all instrumentation
- As-built drawings and schematics
- Operation & maintenance manuals and training records
Beyond new build
We also work on facilities that already exist. Where a plant is being re-audited, expanded or repurposed, we carry out gap analysis against the applicable guideline, identify what will not survive inspection, and execute the remediation across envelope, air system, services and documentation together.
Tell us what you're building.
Share your process, area and target classification, and we'll come back with a design approach and a detailed techno-commercial proposal.