Integrated Clean Room Solution
Complete clean-room delivery — insulated panels, HVAC integration, specialised ducting and electrical systems.
About the Integrated Clean Room Solution
A complete cleanroom is a coordinated build of envelope, HVAC, ducting and electrical — none of which can be done well in isolation. We deliver all four under one contract, sized to your target ISO 14644-1 class. The envelope (PUF / honeycomb panels), the air system (HEPA-filtered AHU, FFU ceiling, return-air risers), the ducts (sealed, smooth-bore stainless or coated steel) and the electricals (sealed conduits, sealed luminaires) are all coordinated to hit and hold the design particle count.
Engineering Advantages
Designed to your target ISO class (typically ISO 5–8 / Class 100–100,000)
Single contract covers envelope + HVAC + ducts + electrical
In-house validation: particle count, recovery time, pressure cascade — full IQ/OQ/PQ documentation
Modular panels mean future expansion or change is a panel-swap, not a rebuild
Key Features
- Insulated panels
- HVAC integration
- Specialised ducting
- Electrical systems
Construction & Materials
- 50 / 75 / 100 mm PUF or aluminium-honeycomb modular panels with concealed fixings
- Coved corners (panel-to-floor and panel-to-ceiling) for cleanability
- HEPA H13 / H14 terminal FFU ceiling
- Stainless or epoxy-coated rigid duct, sealed to SMACNA Seal Class A
- Sealed flush-mount luminaires and IP 65 sockets
- Dedicated pressure-cascade differential gauges per room
How to Choose the Right Variant
- 1Set the target ISO 14644-1 class first — it drives every downstream selection
- 2Specify the recovery time requirement (e.g. 15 min from at-rest to operational class)
- 3Specify required pressure cascade (typically 10–15 Pa per step out from cleanest zone)
- 4Allocate space for return-air risers — never use a corridor as a return path
Installation Notes
- Establish a clean-build protocol from the day panels arrive on site
- Pressure-test ducts to SMACNA before insulating
- HEPA leak-test (PAO/DEHS) every terminal filter at handover
- Run a full validation: particle count, recovery time, pressure cascade, airflow uniformity
Maintenance Schedule
- Particle count monitoring — continuous in pharma cleanrooms
- HEPA integrity test annually; replace when pressure-drop hits design final
- Pre-filters: replace per pressure-drop monitor
- Periodic re-validation per the user's SOP / regulatory cycle
Industries Served
Standards & Compliance
- ISO 14644-1 cleanroom classification
- EU GMP Annex 1 grades A/B/C/D for pharma
- ISO 14644-3 test methods (recovery time, leak test)
- HEPA filtration per EN 1822 H13/H14
Frequently Asked Questions
How do I know what ISO class I need?
Pharma fill/finish is typically ISO 5 (Grade A); pharma compounding ISO 7 (Grade B); medical-device assembly ISO 7–8; semiconductor lithography ISO 3–5. Your regulator or process spec dictates the class.
What is recovery time?
The time taken for the room to return from a disturbed state (lights on, people moving) back to the at-rest particle count. ISO 14644-3 requires < 10–20 min depending on class.
Related Turnkey HVAC — End-to-End Solutions
Need help selecting the right fan?
Our engineers will help you size the integrated clean room solution to your exact application — capacity, static pressure, and installation constraints.
