ISO 14644-1 cGMP, USFDA and EU-GMP ready facilities

We engineer the air your product is made in.

Turnkey cleanrooms, HVAC and MEP under one contract. Designed by our engineers, built in our own plant at Tarapur MIDC, installed and qualified by our site teams.

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Years Specialist Experience
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Integrated Disciplines
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Export Countries
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GMP Compliant Delivery
Who We Are

One partner, from empty shell to validated facility.

Accord Cleanroom Solutions Private Limited is an engineering and manufacturing company specialising in turnkey solutions for cleanrooms and controlled environments.

Our team brings more than a decade of specialist experience in engineering, constructing and manufacturing critical facility elements. We have delivered API, formulation and food industry projects across India and in six export markets. Because we manufacture our own panels, doors, air handling units and cleanroom equipment, we control quality, cost and delivery rather than coordinating them.

  • Single-point responsibility across design, manufacture, installation and qualification
  • In-house factory at Tarapur MIDC, Boisar, Maharashtra
  • Validation-ready DQ, IQ and OQ documentation from day one
  • 24×7 support across the complete facility lifecycle
Quality control laboratory built with modular cleanroom partitions and flush view panels
Representative Modern quality-control laboratory
See The Difference

What separates ISO 5 from ISO 8.

The limits in ISO 14644-1 span three orders of magnitude, which is hard to picture from a table. Select a class below and watch the particle load change.

Counts are the maximum permitted particles at or above 0.5 µm per cubic metre. On-screen density is scaled for legibility.

Selected Class
ISO 7
Max particles ≥0.5 µm/m³: 352,000 Typical ACPH: 60–90 Core manufacturing and processing suites
Why Accord

Compliance is designed in, not inspected in later.

Every facility we build is engineered against the guideline your auditor will actually open. Classification, pressure cascade and documentation are settled at design qualification, so the validation phase confirms the design instead of repairing it.

USFDA UK MHRA EU-GMP WHO-GMP cGMP ISO 14644-1 FS 209E DQ, IQ & OQ

Custom-engineered, never catalogue-fitted

Every facility is engineered around your product, process and compliance goals, from a single room to complete departments.

Factory-built quality control

Panels, doors, AHUs and equipment are manufactured in our own plant, giving controlled quality, shorter delivery and lower cost than site-built alternatives.

Support that outlasts handover

Dedicated after-sales service and validation support through the complete facility lifecycle, with 24×7 client response.

How We Deliver

A ten-stage execution methodology

A structured, validation-ready delivery process that keeps your project audit-proof from day one, running from procurement through to training and handover.

Procurement

Vendor and material finalisation against approved specifications.

Design Qualification

URS translated into an approved, auditable design basis.

Detailed Engineering

Drawings, BOQs, schematics and interface coordination.

Validation Planning

Protocols and acceptance criteria agreed before fabrication.

Equipment Construction

Factory manufacturing of panels, doors, AHUs and equipment.

Factory Testing

FAT completed and signed off before dispatch to site.

Shipping & Installation

Site erection executed by our own installation teams.

Site Testing

SAT, IQ and OQ execution with your quality team.

Documentation

Complete validation dossier compiled and handed over.

Training & Commissioning

Operator training, handover and 24×7 ongoing support.

Common Questions

What clients ask before starting

Both. We work from your User Requirement Specification through design qualification, detailed engineering, manufacturing, installation and validation. If you already have a consultant-issued design, we execute against it. If you do not, we develop the facility layout and design basis with you.

It depends on where your product is exposed and for how long. Rather than over-classifying an entire block, we map your process and assign classes room by room. That typically means ISO 7 or ISO 8 for general manufacturing, with ISO 5 protection only over critical exposed zones. Final classes are frozen jointly with your process team during design qualification.

Modular panels give flush, easy-clean cGMP surfaces that are practically maintenance-free, cost less than civil construction, install far faster, and can be dismantled and reconfigured when your process changes. A civil wall cannot be moved without demolition. A panel wall can.

A complete validation dossier covering design, installation and operational qualification protocols and reports, factory and site acceptance test records, material certificates, as-built drawings and O&M manuals. Protocols and acceptance criteria are agreed before fabrication begins rather than written afterwards.

Yes. We have executed projects across India and exported to Tanzania, Uganda, Ethiopia, Ghana, Nepal and Sri Lanka. Manufacturing is centralised at our Tarapur MIDC plant near Boisar, with installation teams deployed to site.

Start the Conversation

Tell us what you're building.

Share your process, area and target classification, and we'll come back with a design approach and a detailed techno-commercial proposal.