Cleanroom solutions for regulated industries.
Contamination control does not change much between a sterile injectable and a semiconductor wafer. What changes is which contaminant matters, and what the auditor asks to see.
Pharmaceutical & Formulations
Oral solids, liquids, ointments and sterile formulations, designed to the pressure cascade, ACPH and cross-contamination controls that USFDA and EU-GMP inspections examine first.
- Granulation, compression & coating suites
- Sterile and aseptic areas with ISO 5 protection
- Dispensing and sampling booths
- Change rooms, airlocks and material transfer
API & Bulk Drugs
Active pharmaceutical ingredient plants where solvent handling, corrosive exhaust and containment sit alongside classification, and where the HVAC scope has to reconcile all three.
- Scrubbed and balanced process exhaust
- Chemical-resistant finishes and flooring
- Containment and potent-compound areas
- Solvent-handling ventilation strategy
Biotechnology
Fermentation, cell culture and downstream processing, including biosafety containment where the risk runs outward from the process rather than inward toward it.
- Biosafety cabinets, Class I & II
- Negative-pressure containment suites
- Media and buffer preparation areas
- Controlled cold and incubation rooms
Electronics & Precision
Assembly and test environments where a settled particle is a permanent yield defect, and where electrostatic discharge is as serious a contaminant as dust.
- ESD-safe flooring, benches and furniture
- Tight temperature stability for metrology
- Laminar protection over critical stations
- Vibration-aware layout and detailing
Food & Beverage
Hygienic processing and packing environments where microbial control, wash-down durability and allergen segregation drive the design as much as particle count.
- Wash-down-rated finishes and drainage
- Positive pressure over non-classified areas
- Chilled and controlled-temperature rooms
- High-care and low-care zone separation
Healthcare & Laboratories
Operating theatres, sterile services, and quality control and analytical laboratories, where the environment supports clinical outcomes and data integrity alike.
- Modular operation theatre environments
- CSSD and sterile supply areas
- QC, analytical and microbiology labs
- Laboratory furniture and fume extraction
Also delivered for
What changes between industries
The engineering discipline stays constant. The controlling variable does not, and getting that wrong is what produces a compliant facility that still cannot make product reliably.
| Sector | Typical Class | Primary Control Driver |
|---|---|---|
| Sterile pharmaceutical | ISO 5 in ISO 7 | Viable and non-viable particle control at the point of exposure |
| Oral solid dosage | ISO 8 | Cross-contamination and dust containment between products |
| API & bulk drugs | ISO 8 / controlled | Exhaust balance, solvent handling and chemical resistance |
| Biotechnology | ISO 7–8 + containment | Directional containment, protecting the operator and the environment |
| Electronics | ISO 5–7 | Particle settlement, ESD and temperature stability |
| Food processing | ISO 8 / hygienic | Microbial control, wash-down durability and allergen segregation |
| Healthcare & labs | ISO 7–8 | Air quality for clinical outcome and analytical data integrity |
Indicative only. Final classification is frozen jointly with your process and quality teams during design qualification.
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.