From concept design and construction to validation and certification — MILES builds ISO 14644 and GMP-compliant cleanrooms for pharmaceutical, semiconductor, food and healthcare clients across Europe, the Middle East and Africa.
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MILES turnkey cleanroom project — pharmaceutical facility, China
Managing multiple vendors for design, construction, equipment and validation is slow and risky. MILES delivers the entire cleanroom lifecycle under one contract — one point of accountability, faster delivery, lower total cost.
Our engineers design to ISO 14644, EU GMP Annex 1 and FDA cGMP requirements — airflow, pressure cascades and HVAC sized right from day one.
Panels, doors, windows and FFUs are produced in our Suzhou factory — better cost control, shorter lead times, consistent quality.
Flat-packed modular systems ship worldwide. Typical timeline from design approval to handover: 12–20 weeks.
We test, balance and certify every cleanroom to its target ISO class — and stay available for filters, spares and requalification.
GMP-compliant sterile suites, fill-finish areas and QC labs up to ISO Class 5 / Grade A.
Explore solution →ESD-safe, vibration-controlled cleanrooms from ISO Class 1 to 8.
Explore solution →Hygienic packaging and processing environments that pass HACCP and BRCGS audits.
Explore solution →Operating theatres, ICU isolation rooms and CSSD with validated pressure regimes.
Explore solution →Containment labs, negative-pressure rooms and precision research environments.
Explore solution →Send us your industry and floor area — an engineer will recommend the right class and layout.
Ask an engineer →Share your requirements; we assess your site remotely or on-site.
Layout, airflow and HVAC design with fixed, transparent pricing.
Panels, doors and equipment produced with full QC records.
Supervised installation by our engineers or certified partners.
Particle testing, certification reports and operator training.
We routinely deliver ISO Class 1–8 cleanrooms and GMP Grade A–D areas, validated with full documentation.
Standard modular cleanrooms: 12–20 weeks from design approval. Large GMP suites: 3–6 months.
Yes — we send engineers for supervision or full installation, and work with certified local partners across Europe, the Middle East and Africa.
Yes. Panels, FFUs, filters, air showers and doors are available as standalone orders with worldwide shipping.
Send us your requirements — floor area, target cleanliness class and industry. Our engineers respond within 24 hours with initial layout suggestions and a budget range.
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