iClean - Integrated Cleanroom TechnologiesiClean - Integrated Cleanroom Technologies
Takasago Thermal EngineeringTakasago Thermal Engineering
TAKASAGO THERMAL ENGINEERING (JAPAN)×iClean Alliance
CFD Airflow: 0.45 m/s Laminar

Pioneering Turnkey Cleanrooms &
Controlled Environments

Integrated Cleanroom Technologies (iClean) delivers mission-critical modular cleanroom envelopes, precision HVAC contamination control, and ultra-dry rooms (<1% RH) for high-stakes industries worldwide.

Select Demanding Industrial Domain
ENGINEERED SPECIFICATION

Aseptic Filling Suites & Sterile Formulation Envelopes

Explore Solution
Cleanroom ClassificationISO Class 5 (Grade A)
Pressure Differential+15 to +30 Pa Cascade
Moisture / RH Precision45% ± 5% RH
Compliance StandardWHO-GMP & US-FDA 21 CFR 211
CFD Verified • ISO 14644-1 Annex 1 Ready
Real-time Architectural Envelope
1,250+Cleanrooms DeliveredAcross 25+ countries globally
20+Years ExcellenceFounded in 2003 in Hyderabad
< 1%Relative Humidity (RH)EV Battery Dry Rooms (-60°C Dew Point)
ISO 1-9Full Spectrum ClassesWHO-GMP & US-FDA compliant
5Manufacturing HubsState-of-the-art CNC automated lines
GLOBAL SYNERGY & JAPANESE PRECISION

Indo-Japanese Engineering Synergy

The alliance between Integrated Cleanroom Technologies and Takasago Thermal Engineering (Japan) unites two decades of turnkey cleanroom agility with a century of thermal engineering leadership.

Takasago Thermal Engineering Co. Ltd. (Japan)

Listed on the Tokyo Stock Exchange (Prime Market 1969.T), Takasago brings over a century of precision thermal engineering and patented cleanroom airflow technologies to iClean’s turnkey project execution across the globe.

Est. 1923 • 100+ YearsTokyo Stock Exchange (Prime: 1969.T)Visit TTE Global Corporate

Centennial Thermal Expertise

Backed by Takasago Thermal Engineering’s century-long innovation in HVAC thermodynamics, cleanroom aerodynamics, and mega-scale industrial facilities.

Turnkey Indian Manufacturing Power

Five advanced automated manufacturing plants across India featuring CNC punch-presses, automated insulated panel roll-forming, and conveyorized powder-coating.

TCR-SWIT® Energy Optimization

Patented swirling induction airflow technology cutting cleanroom HVAC electrical consumption by up to 30% while maintaining Grade A cleanliness.

Strict Quality & EHS Governance

Integrated Japanese 5S, Kaizen, and global ISO standards ensuring contamination-free handovers on fast-track turnkey project schedules.

ENGINEERED CONTAMINATION CONTROL

Turnkey Cleanroom Solutions

From modular architectural envelopes to precision air handling and biosecurity isolators, explore our core cleanroom divisions.

Core Division

Modular Architectural Envelopes

GMP-compliant partitions, walk-on ceilings & hermetic doors

Factory-engineered modular wall panels and ceiling systems engineered for rapid on-site assembly with airtight silicone flush joints and anti-microbial finishes.

  • Progressive & non-progressive modular wall panels with PIR / Rockwool / Aluminium honeycomb cores
  • Heavy-duty walk-on ceiling grid supporting maintenance loads up to 150 kg/m²
  • Hermetic cleanroom doors with automatic drop-down bottom seals and interlock controls
  • Flush double-glazed view windows with desiccated silica gel to prevent condensation
Contamination Control

Precision HVAC & Cleanroom Equipment

Airflow handling, filtration & dynamic pass boxes

State-of-the-art cleanroom containment equipment engineered with HEPA/ULPA filtration (H14/U15) ensuring laminar airflow and zero particulate cross-contamination.

  • Dynamic & Static Pass Boxes (DPB/SPB) with UV germicidal lamps and electromagnetic interlocks
  • Laminar Air Flow (LAF) workstations and mobile sterile battery-backup transfer trolleys
  • Class II Type A2 & B2 Bio-Safety Cabinets for sterile cytotoxic & biological handling
  • Dispensing and sampling reverse-laminar booths protecting operator, product & environment
EV & Energy Transition

EV Battery Dry Rooms (<1% RH)

Ultra-low dew point engineering for Lithium-ion cells

Specialized ultra-low moisture environments operating at dew points from -40°C down to -60°C (<1% Relative Humidity), critical for Lithium-ion battery gigafactories.

  • Hermetically sealed vapor-barrier modular wall & ceiling panels with thermal breaks
  • Desiccant chemical rotor dehumidification integrated with Takasago precision refrigeration
  • Personnel airlocks and material transition chambers with rapid moisture recovery
  • Energy-efficient return air recirculators designed for high volume dry room airflow
High Containment

Biosecurity Labs & Mobile Virology Units

BSL-3/BSL-4 biocontainment, mist showers & mobile labs

High-containment engineering meeting strict CDC and WHO BSL-3 / BSL-4 guidelines for high-risk pathogen research, vaccine manufacturing, and emergency outbreak response.

  • Container-based and bus-based mobile BSL-3 virology laboratories for field deployment
  • High-velocity personnel Air Showers and chemical Mist Decontamination Showers
  • Inflatable pneumatic seal doors for airtight gas-tight decontamination suites
  • Negative pressure cascade systems with dual HEPA exhaust safe-change bag-in/bag-out (BIBO)
SECTOR-SPECIFIC EXPERTISE

Industries We Empower

Our cleanrooms safeguard mission-critical processes across the world’s most demanding technological sectors.

750+ Facilities

Pharmaceuticals & Injectables

WHO-GMP & US-FDA (Grade A to D)

Sterile formulation suites, API synthesis, sterile injectables, and oral solid dosage cleanroom facilities.

ISO Class 1 Capable

Semiconductor & Microelectronics

ISO 14644-1 (ISO Class 1 to 5)

Sub-micron particulate control, static-dissipative ESD flooring, vibration isolation, and toxic gas exhaust systems.

Gigafactory Scale

EV Lithium-Ion Battery Fabs

<1% RH (-40°C to -60°C Dew Point)

Hermetic dry rooms for cathode/anode slurry coating, cell assembly, electrolyte filling, and aging chambers.

250+ Biotech Suites

Biotechnology & Vaccines

BSL-2 / BSL-3 / BSL-4 Containment

Monoclonal antibodies, cell & gene therapy suites, vaccine fill-finish, and fermentation containment envelopes.

Zero-Bioburden Tech

Medical Devices & Implants

ISO 13485 & ISO Class 7/8

Controlled assembly spaces for orthopaedic implants, cardiovascular stents, catheters, and surgical packaging.

High-Bay Facilities

Aerospace & Precision Optics

ISO Class 5 to 7 Outgassing Spec

Satellite integration halls, optical laser calibration cleanrooms, and space exploration payload packaging.

FULL LIFECYCLE EPC CAPABILITIES

Our 5-Stage Turnkey Execution

From concept airflow simulation to validation handover, our single-source accountability accelerates your time-to-market.

01

Consultation & CFD Simulation

Cleanroom zoning, pressure cascade calculation, personnel flow optimization, and Computational Fluid Dynamics (CFD) airflow modeling.

02

Precision CNC Manufacturing

Automated fabrication of insulated panels, walk-on ceilings, dynamic pass boxes, and doors across 5 modern production plants.

03

Cleanbuild Rapid Installation

Certified cleanroom engineers assemble flush envelopes using Cleanbuild protocols to avoid on-site contamination.

04

HVAC Commissioning & BMS

Airflow balancing, HEPA filtration integration, chilled water testing, and automated Building Management System (BMS) setup.

05

Validation & Regulatory Handover

Comprehensive DQ/IQ/OQ/PQ protocols, DOP/PAO filter integrity tests, particle count certifications, and full audit documentation.

MARQUEE GLOBAL PARTNERS

Trusted by Industry Leaders Worldwide

Over 1,250 cleanroom projects successfully commissioned for premier pharmaceutical, healthcare, and technology corporations across the globe.

Dr. Reddy's LaboratoriesPharmaceuticals
Sun PharmaPharmaceuticals
CiplaRespiratory & Pharma
Bharat BiotechVaccine Manufacturing
Serum Institute of IndiaImmunology
Hetero DrugsAPI & Generics
Aurobindo PharmaSterile Injectables
Biocon BiologicsBiosimilars
Foxconn Technology GroupElectronics Manufacturing
Tata ElectronicsPrecision Semiconductor
Reliance Life SciencesBiotechnology
Lupin PharmaceuticalsGlobal Formulation
Global Footprint Across 25+ Nations
Turnkey installations validated to US FDA, WHO-GMP, and EU GMP standards worldwide.
North America (USA)European UnionJapanMiddle East (UAE/KSA)Southeast AsiaIndia
VALIDATED COMPLIANCE & STANDARDS

Certified to Global Cleanroom Benchmarks

ISO 14644-1Cleanroom Air Cleanliness ClassificationISO Class 1 to Class 9
WHO-GMPGood Manufacturing PracticesGlobal Health Authority Compliance
US FDA 21 CFR 211Federal cGMP ComplianceSterile Drug Processing Guidelines
EU-GMP Annex 1Manufacture of Sterile ProductsGrade A, B, C & D Airflow Standards
ISO 9001:2015Quality Management SystemsCertified Precision Manufacturing
ISO 14001:2015Environmental ManagementEco-conscious Low-Carbon Footprint
ISO 45001:2018Occupational Health & SafetyZero-Accident Cleanbuild Standard
FREQUENTLY ASKED QUESTIONS

Cleanroom Engineering FAQ

Insights into ISO classifications, EV battery dry rooms, turnkey EPC execution, and modular reconfigurability.

iClean designs, manufactures, and validates cleanrooms across the entire ISO 14644-1 spectrum, from ISO Class 1 (ultra-critical sub-micron semiconductor fabs) to ISO Class 9, as well as WHO-GMP and EU-GMP Grades A, B, C, and D for sterile pharmaceuticals.
GET IN TOUCH WITH OUR SPECIALISTS

Ready to Build or Upgrade Your Controlled Environment?

Consult with our turnkey cleanroom engineers to specify modular wall & ceiling panels, precision HVAC contamination control, or ultra-low dew point EV dry rooms tailored to your regulatory standards.