Cleanroom Projects & Turnkey Solutions.
From design to validation — we take complete assignments for ISO Class 5 to ISO Class 8 cleanrooms, and can deliver every equipment package the facility needs as one turnkey scope.
ISO Class 5 to ISO Class 8.
Critical aseptic zones, filling, LAF and RABS/isolator environments.
Sterile support, device assembly and high-grade process rooms.
Cleanroom manufacturing, assembly, packaging and change suites.
Support corridors, material airlocks, warehousing and secondary packing.
Regulated environments across four sectors.
Cleanroom projects for pharma and biopharma, semiconductor and electronics, hospitals and healthcare, and medical device, cell & gene therapy and research facilities.
Pharma & Biopharma
Sterile and non-sterile formulation, OSD, biologics, fill-finish, QC and microbiology laboratories.
Semiconductor & Electronics
Assembly, inspection, packaging and precision electronics rooms with tight particle and ESD control.
Hospitals & Healthcare
Operation theatres, ICUs, IVF and stem-cell labs, compounding pharmacies and CSSD areas.
Medical Devices, CGT & Research
Device assembly suites, cell & gene therapy cleanrooms, research and academic facilities.
Design, build, equip, validate.
A complete scope under one project manager — or any part of it, if your team already owns the rest.
Design & Engineering
Concept layouts, personnel and material flow, room classification, pressure cascade, airflow and load calculations, GMP-aligned design documentation.
Civil & Cleanroom Build
Modular partitions and ceilings, coved epoxy or vinyl flooring, doors, view panels, pass boxes, air showers and change rooms.
HVAC & Utilities
AHUs, HEPA terminal filtration, ducting, BMS/EMS integration, compressed air, purified water, gases, electricals and lighting.
Turnkey Equipment Package
Process, laboratory and support equipment for the industry — specified, supplied, installed and integrated as one package.
Qualification & Validation
DQ/IQ/OQ/PQ protocols, air velocity, HEPA integrity, particle counts, recovery and pressure studies, cleanroom classification reports.
Handover & AMC
Documentation dossier, operator training, spares, filter replacement and periodic requalification under annual maintenance contracts.
Six stages from brief to classified room.
Every stage has defined deliverables, documentation and sign-off, so qualification is a confirmation rather than a discovery.
Requirement & Feasibility
Product, process, classification targets, site survey, statutory requirements and budget framing.
Concept & Detailed Design
Layouts, flows, HVAC schemes, equipment list, URS and specification freeze with your technical team.
Procurement & Fabrication
Vendor qualification, panel and HVAC fabrication, equipment ordering with delivery tracking.
Execution at Site
Sequenced installation of partitions, flooring, HVAC, utilities and equipment under a single project manager.
Commissioning & Qualification
Balancing, integrity testing, protocol execution and classification to the target ISO class.
Handover & Support
As-built drawings, validation dossier, training and continuing maintenance and requalification support.
Built by a team that works in cleanrooms.
One accountable partner
Design, build, equipment and validation under one contract — no gaps between the cleanroom vendor, the HVAC contractor and the equipment supplier.
Cleanroom operators, not just contractors
We run our own ISO Class 7 cleanroom operations daily, so the rooms we build are designed for how they will actually be used and cleaned.
Validation-first engineering
Classification, recovery and pressure performance are designed in from the first drawing, not chased after handover.
Equipment and consumables continuity
Filtration, contamination control consumables, lab equipment and hose assemblies continue from the same team after handover.
Share your layout and target class — we respond within 2 business days.
Send the available area, process description, target ISO class and timeline. Our engineers return a concept scheme, equipment outline, validation scope and indicative budget.
Build with India's cleanroom hose assembly and OEM manufacturing partner.
Tell us what you need to manufacture. Our engineering team will scope your assembly, packaging, and quality requirements within 2 business days.