Turnkey cleanrooms, engineered and validated to standard
From modular panels and GMP doors to HEPA-filtered HVAC and documented validation — we build controlled environments that pass audit, not just inspection.
A single team for the whole cleanroom, not just the air
A cleanroom only performs when the envelope, the airflow and the controls are designed as one system. We take that on end to end — engineering the room layout and pressure cascade, manufacturing the panels, doors and pass boxes, installing the HVAC and HEPA filtration, and validating the finished suite with the documented test data your compliance team signs off.
The result is a controlled environment built to hold its class in operation — for pharmaceutical, healthcare, electronics and industrial processes where particle count, pressure and airflow are non-negotiable.
Built to the class your process demands
We design and validate cleanrooms across the full ISO 14644 and GMP range — matching cleanliness, pressurisation and airflow to the operation inside.
ISO 5
Grade A / B
Aseptic filling and sterile core zones — laminar-flow, unidirectional air over the critical process.
ISO 6
Grade B
Background to aseptic operations and sterile support areas with tight particle and pressure control.
ISO 7
Grade C
Solid dosage, compounding, dispensing and preparation rooms with cascaded pressurisation.
ISO 8
Grade D
Primary packing, secondary manufacturing, gowning and controlled storage / warehousing.
Every element of the controlled environment
Envelope, equipment and controls — designed, manufactured and installed to work together.
Modular Wall & Ceiling Panels
PUF / rockwool sandwich panels with flush-glazed view panels and coved skirting for a particle-free, wipe-down envelope.
GMP Doors & View Panels
Flush, interlocking hinged and sliding GMP doors with vision panels, door interlocks and sweep seals.
Epoxy & PU Flooring
Self-levelling, seamless anti-static epoxy and PU coved flooring that stands up to cleaning chemicals.
HEPA Filtration & FFUs
Terminal HEPA boxes, fan filter units and laminar-flow hoods delivering ISO 5–9 class air at the workface.
AHUs & Air Distribution
Double-skin AHUs, treated-fresh-air units, low-level return risers, diffusers and dampers sized for required ACPH.
Pass Boxes & Dynamic Hatches
Static and dynamic pass boxes with interlocks and UV, plus material and personnel airlocks.
Air Showers & Gowning
Personnel and cargo air showers, gowning rooms and change-room sequencing that keep contamination out.
Pressurisation & BMS Controls
Room-to-room pressure cascades, magnehelic gauges and BMS-monitored temperature, RH and differential pressure.
Lab Furniture & Equipment
Stainless steel tables, biosafety cabinets, laminar airflow units and pass-through storage for the clean core.
Proven on paper, not just promised
Installation is not finished until it is measured. Every cleanroom is handed over with documented qualification data.
Non-Viable Particle Count
At-rest and in-operation particle counts to confirm the ISO / GMP class.
HEPA Filter Integrity (PAO/DOP)
Aerosol challenge and scan of every terminal filter and housing seal.
Air Velocity & ACPH
Face velocity and air changes per hour verified against the design basis.
Room Pressurisation
Differential-pressure cascade mapped room-to-room and against ambient.
Airflow Visualisation
Smoke studies proving unidirectional flow and no dead zones over the process.
Recovery & Cleanup Rate
Time to recover class after a challenge, documented for the qualification report.
Controlled environments for every regulated sector
Pharmaceutical & Sterile
Aseptic filling, tablet, injectable and API suites to WHO-GMP and Schedule M.
Hospitals & Healthcare
Modular operation theatres, ICUs and hospital pharmacies with HEPA-filtered air.
Electronics & Semiconductors
Low-particle assembly and inspection rooms with anti-static, ESD-safe finishes.
Food, Nutra & Cosmetics
Hygienic processing and packing halls that meet FSSAI and export audit norms.
Biotech & R&D Labs
BSL-graded labs, tissue-culture and research suites with biosafety containment.
Medical Devices
Class 7–8 assembly and sterile-barrier packaging lines to ISO 13485 workflows.
From requirement to a qualified cleanroom
Requirement & URS Study
We capture your process, product and regulatory class, then translate it into a user requirement specification.
Design & Engineering
Room layouts, pressure cascade, HVAC load and HEPA scheme are engineered and issued as coordinated GA / MEP drawings.
Manufacturing & Supply
Panels, doors, pass boxes and air-handling equipment are fabricated to the approved specification.
Installation & Fit-Out
Envelope, flooring, HVAC and utilities are installed and sealed by our site teams to GMP standards.
Validation & Handover
The suite is tested, balanced and qualified — with the documented reports your compliance team signs off.
Cleanrooms we have delivered
Answers before you ask
Both. We can deliver the complete turnkey envelope — panels, doors, flooring, HVAC, utilities and validation — or design and install only the cleanroom HVAC and filtration if your civil work is handled separately.
We design and validate cleanrooms from ISO 5 to ISO 9 (EU/WHO-GMP Grade A to D), including aseptic Grade A/B suites with unidirectional laminar flow.
Yes. On completion we hand over qualification reports — particle counts, HEPA integrity (PAO/DOP), air velocity and ACPH, pressurisation, airflow visualisation and recovery — so your team can close out DQ/IQ/OQ.
Our cleanrooms are built to ISO 14644 for classification and cleanliness, and to WHO-GMP / EU-GMP and Schedule M for pharmaceutical facilities, with finishes chosen to suit the applicable audit norms.
Our base is Delhi NCR and that is where we work fastest, but we take up cleanroom and HVAC projects for pharma and industrial clients across the region — tell us the location and we will confirm.
Planning an HVAC or cleanroom project?
Talk to our engineering team about design, installation or AMC support — we'll respond with a clear scope and quote.