Four rooms. Four different sets of rules.

All of them decided above the ceiling.

Turnkey cleanroom engineering

Turnkey cleanrooms for India’s most critical industries

01 / Pharmaceutical

Sterile suites that hold their grade on audit day

A pharmaceutical cleanroom has to prove itself twice. Once when we hand it over, and again every time an inspector walks the floor.

EU-GMP Grade A to DISO Class 5 to 8Positive pressure cascade
Pharmaceutical cleanrooms
02 / Semiconductor & Electronics

A room where one particle costs you a wafer

Chip and electronics lines fail on contamination nobody can see, so the room is built to catch it before it ever lands.

ISO Class 4 to 6FFU and T grid ceilingVertical laminar flow
Semiconductor cleanrooms
03 / Solar & Renewables

Clean space at the scale a module line actually runs at

Solar is a volume problem before it is a cleanliness problem. Holding one very large bay clean while it runs at full output is harder than holding a small one.

ISO Class 7 to 8High air change rateConveyor and robotics ready
Solar cleanrooms
04 / Containment & Biosafety

Some rooms exist to keep what is inside from getting out

Containment reverses the logic. Instead of protecting the product from people, the room protects people from the product.

Negative pressureSealed HEPA exhaustInterlocked airlocks
Containment and biosafety
05 / Cleanroom HVAC

Cleanroom HVAC is what turns a room into a cleanroom

Every room you just walked through depends on the plant above it. This is where the air is conditioned, filtered, balanced and held.

AHU design and manufactureH13 and H14 terminal HEPAPressure and RH control
Cleanroom HVAC
Our clients

Trusted across India's most regulated industries

Cleanrooms delivered for India's leading drug makers, electronics manufacturers and national institutions, from ISRO and BARC to Cipla, Sun Pharma and Pfizer.

Ajanta Pharma
Anthem Biosciences
Aurobindo Pharma
Baidyanath
Cadila Pharmaceuticals
Cipla
Emami
Glenmark
Hamdard
Intas Pharmaceuticals
Lupin
Mankind Pharma
Micro Labs
Mylan
P&G
Pfizer
Reliance Life Sciences
Schott Poonawalla
Strides
Ajanta Pharma
Anthem Biosciences
Aurobindo Pharma
Baidyanath
Cadila Pharmaceuticals
Cipla
Emami
Glenmark
Hamdard
Intas Pharmaceuticals
Lupin
Mankind Pharma
Micro Labs
Mylan
P&G
Pfizer
Reliance Life Sciences
Schott Poonawalla
Strides
Sun Pharma
Torrent Pharmaceuticals
Unichem Laboratories
USV
Zydus
Alembic
Bosch
BARC
Exide
HAL
ICMR
ISRO
Jhalawar Medical College
NISER
Siemens
Parker
Sopee Paediatric Hospital
HBCHRC, New Chandigarh
TDK EPCOS
Sun Pharma
Torrent Pharmaceuticals
Unichem Laboratories
USV
Zydus
Alembic
Bosch
BARC
Exide
HAL
ICMR
ISRO
Jhalawar Medical College
NISER
Siemens
Parker
Sopee Paediatric Hospital
HBCHRC, New Chandigarh
TDK EPCOS
One accountable partner

One partner, from design to validated handover

Most cleanroom projects are stitched together from a designer, a panel supplier, an HVAC contractor and a validation agency, and the gaps between them are where schedules slip and audits fail.

Fabtech does all of it in-house: cleanroom design and build, modular wall and ceiling systems, cleanroom HVAC, epoxy flooring and validation. One partner, one accountable team, one ISO 14644 environment that qualifies the first time.

The usual way, 4+ contracts
Cleanroom designer
Panel supplier
HVAC contractor
Epoxy / flooring
Validation agency
Fabtech CleanroomsOne accountable team
One partner, delivered
One partner, one team
ISO 14644 environment
Qualifies the first time
Audit-ready dossier
2,000+
Cleanrooms delivered
8
Critical industries
20+
Years of cleanroom engineering
1
Team, design to validated handover

The accounts, the board and the filings are on record, so your procurement and audit teams can check us themselves before anything is signed.

Investor relations

What we deliver

Turnkey cleanroom solutions, end to end

Design, manufacture, install, validate, and maintain. Scroll through the full lifecycle.

Scroll
How we work

How we deliver a validated cleanroom

One accountable team across six stages, so the gaps where projects fail never open.

  1. 01

    Consult & Feasibility

    We begin by capturing your User Requirement Specification (URS), surveying the site, and fixing the ISO class and EU-GMP grade your process needs. You leave this stage with a realistic investment, a delivery programme and a bounded scope, so the project starts from a fixed target instead of an assumption.

  2. 02

    Design & DQ

    Our engineers develop the room layout, airflow scheme and pressure-cascade design, then select the HVAC and process equipment to match. Every decision is recorded in a formal Design Qualification, so the cleanroom is proven against your requirements on paper before a single panel is manufactured.

  3. 03

    Manufacture

    Panels, HVAC components and equipment are built to specification in our own facilities, not sub-contracted out. Each assembly passes Factory Acceptance Testing (FAT) before it leaves the floor, so what arrives at your site fits and performs the first time, with no improvised rework.

  4. 04

    Install & IQ

    Our site teams handle construction and integrate all services, then document the build through Installation Qualification. IQ confirms the cleanroom has been installed and connected exactly as designed, creating the verified baseline we commission and validate against.

  5. 05

    Commission & Validate

    We run Operational and Performance Qualification with HEPA integrity (PAO/DOP) testing, particle counts, recovery studies and smoke and airflow visualisation. The result is a validated environment, handed over with the certification data your auditors and regulators will ask to see.

  6. 06

    Handover & AMC

    At handover you receive complete as-built documentation, the full validation dossier and operator training. Our Annual Maintenance Contracts then keep the facility in qualified condition through scheduled servicing, filter management and periodic requalification, protecting the investment for years.

In-house manufacturing

Cleanroom equipment, built in-house

PRODUCT 01

Laminar Air Flow Units

Horizontal & vertical LAF, ISO Class 5 zones

Horizontal and vertical clean benches that bathe the work zone in unidirectional HEPA-filtered air, holding ISO Class 5 over the critical area for sterile handling and sampling.

PRODUCT 02

Fume Hoods

Ducted, ductless & chemical-resistant

Ducted, ductless and chemical-resistant hoods that capture fumes and vapours right at the face and exhaust them safely, protecting both the operator and the process.

PRODUCT 03

Pass Boxes

Static, dynamic & VHP

Static, dynamic and VHP transfer hatches that move material between classified zones through interlocked doors, so the air seal between grades is never broken.

PRODUCT 04

Cleanroom Doors

Flush, interlocked, view-panel

Flush, interlocked, view-panel doors engineered to be fully cleanable and airtight, holding the pressure cascade between adjacent classified rooms.

PRODUCT 05

HEPA Filtration & FFUs

H13/H14 fan-filter units & housings

H13 and H14 fan-filter units and filter housings that deliver the air changes and cleanliness your classification demands, ceiling-mounted and serviceable from the room.

PRODUCT 06

Modular Panels

Wall & ceiling systems

Flush wall and ceiling panel systems with coved corners and flush glazing, built for GMP cleanability and fast, low-disruption installation.

PRODUCT 07

Air Showers

Personnel & material entry

Personnel and material air showers that strip loose particles off gowns and carts with high-velocity HEPA-filtered jets before anything enters the cleanroom.

PRODUCT 08

Biosafety Cabinets

Class II microbiological safety

Class II microbiological safety cabinets that protect the operator, the product and the environment at once, with HEPA-filtered downflow and exhaust.

Standards

How clean is clean enough

Cleanrooms are graded by how many particles a cubic metre of air is allowed to hold. Each step down the ISO 14644 scale cuts that budget by a factor of ten, and that single number sets the filters, the air changes and the pressure the room runs at.

Find your class:

Particles 0.5 µm and larger, per cubic metre of air

3,520
35,200
352,000
3,520,000
ISO Class 5
ISO Class 6
ISO Class 7
ISO Class 8

Each step allows ten times the particles of the one before it.

Pharmaceutical work sits at ISO Class 5 in the aseptic core and ISO Class 7 in the space around it. Semiconductor lines run cleaner again. Solar, food and beverage and general GMP production sit at ISO Class 8. Pharmaceutical rooms carry a second grade on top of the ISO class, EU-GMP Grade A to D, and the two scales line up with each other.

The full ISO Class 1 to 9 table, the EU-GMP map and the legacy Class 100 to Class 100,000 names live on the classification page.

See cleanroom classification in depth

Industries we serve

Built for the industries that can't afford failure

Sector agnostic, one standard of control. Each industry comes with its own regulations, particle limits and pressures, and we engineer to all of them.

Engineered to the standards your auditors demand

Every cleanroom is designed, built and validated to the framework your facility will be audited against. Documented and traceable.

ISO 9001
ISO 14001
ISO 45001
WHO-GMP alignment
India Schedule M
EU-GMP Annex 1
cGMP readiness
ISO 14644 testing
Engineering validation

Cleanrooms for the names you know

From national research institutions to India's largest drug makers, our work runs inside the country's most regulated facilities.

Selected clients

In their words

Trusted by India's regulated manufacturers

Pharma, API and consumer-care leaders on what it is like to build a cleanroom with Fabtech.

Pharma
Fabtech completed the cleanroom project at our Plant 16, Ankleshwar site within the timeline. We extend our thanks to all the staff involved, and assure them they will be considered for Glenmark's future projects.
GP
Vishal Jain
Sr. Manager - Projects
Glenmark Pharmaceutical Ltd.
API
Fabtech successfully completed our API pilot-plant expansion at our Vizag plant to our satisfaction in terms of quality, timelines and safety standards. The entire team demonstrated a very good attitude and cooperation.
EP
Anand Galphade
Sr. Director - Project & Execution
Eisai Pharmaceutical India Pvt. Ltd.
Consumer Care
We award this certificate to Fabtech for their outstanding performance and efforts towards the successful completion of the modular cleanroom project for our Sangli project. We wish them all the best for their future ventures.
RC
Vinay Wagh
Head - Factory
Rajaram Consumer Care Pvt. Ltd.
Pharma
We highly appreciate the efforts the Fabtech team put in to overcome hurdles during execution. Their ability to work through unforeseen challenges and their collaborative approach is impressive. We have had excellent support from the entire team.
NL
Project Team
Engineering
Nichepharm Lifescience Pvt. Ltd.
Pharma
Fabtech completed the cleanroom project at our Plant 16, Ankleshwar site within the timeline. We extend our thanks to all the staff involved, and assure them they will be considered for Glenmark's future projects.
GP
Vishal Jain
Sr. Manager - Projects
Glenmark Pharmaceutical Ltd.
API
Fabtech successfully completed our API pilot-plant expansion at our Vizag plant to our satisfaction in terms of quality, timelines and safety standards. The entire team demonstrated a very good attitude and cooperation.
EP
Anand Galphade
Sr. Director - Project & Execution
Eisai Pharmaceutical India Pvt. Ltd.
Consumer Care
We award this certificate to Fabtech for their outstanding performance and efforts towards the successful completion of the modular cleanroom project for our Sangli project. We wish them all the best for their future ventures.
RC
Vinay Wagh
Head - Factory
Rajaram Consumer Care Pvt. Ltd.
Pharma
We highly appreciate the efforts the Fabtech team put in to overcome hurdles during execution. Their ability to work through unforeseen challenges and their collaborative approach is impressive. We have had excellent support from the entire team.
NL
Project Team
Engineering
Nichepharm Lifescience Pvt. Ltd.

We don't disappear at handover

Filters load and equipment drifts over time. After handover the cleanroom is yours to run, and our equipment AMC keeps the systems we supplied — HEPA filters, LAF units and HVAC — performing and requalified, so the room holds its class year after year.

HEPA replacement
Periodic revalidation
Particle-count re-testing
Preventive HVAC upkeep
Equipment AMC
Ticker: FABCLEAN

A company you can check before you sign

Financial results, annual reports, shareholding and governance are all published, and all here, the due-diligence trail your procurement and audit teams already rely on.

FABCLEANBSE listing
FABCLEANLive on BSE

Live share price is published on the exchanges.

The group

Three companies alongside this one

Fabtech Cleanrooms holds a disclosed equity stake in Kelvin, AART and Advantek. Air conditioning and ventilation, facility and utility engineering design, and air handling units. Your cleanroom stays with Fabtech Cleanrooms either way.

Fabtech Cleanrooms

Fabtech Cleanrooms and the three companies it holds a disclosed equity stake in. Schematic, not a shareholding statement.

  • Kelvin

    Air conditioning and ventilation. The HVAC side of a controlled environment, from the plant room to the terminal.

  • AART

    Facility and utility engineering design for semiconductor and advanced manufacturing, with a working footprint across Europe and Asia.

  • Advantek

    Air handling units. The machine that conditions and moves the air a cleanroom depends on.

Which Fabtech you are dealing with
Visit us

Headquartered in Mumbai, manufacturing in three states

Our design, engineering and project teams run out of Andheri, Mumbai, and on site at regulated facilities nationwide. The equipment they specify is made in our own plants in Gujarat, Telangana and Maharashtra.

Umbergaon
Gujarat

Dedicated cleanroom production, roughly 6,500 square metres

Hyderabad
Telangana

Manufacturing for southern and central India

Thane
Maharashtra

Manufacturing within the Mumbai metropolitan region

Head office
Fabtech Cleanrooms
615, Janki Centre, Off Veera Desai Road, Andheri (West),
Mumbai, Maharashtra 400053, India
+91 22 6159 2900quote@fabtechnologies.comGet directions
Listed BSE: FABCLEAN
Request a quote

Tell us about your cleanroom

Share your industry, ISO class and floor area. Our engineers respond with a scoped proposal, not a brochure.

Based in Andheri (West), Mumbai
Delivering cleanroom projects across India.

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