ISO 9001 & GMP Certified

Leading Clean Room & Pharmaceutical Validation Experts

End-to-end design, construction, HVAC systems manufacturing, and regulatory compliance validation for critical environments.

ISO 14644 Compliant
GMP Standards
US FDA Audited
WHO Standards
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Projects Completed
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Cleanrooms Built
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Annual Validations
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Expert Engineers
Comprehensive Capabilities

Our Cleanroom & Validation Services

We deliver high-precision engineering solutions tailored to pharmaceutical and containment guidelines.

Clean Room Solutions

Clean Room Solutions

Turnkey design, supply, and installation of modular wall partitions, ceilings, doors, and pass boxes to meet strict ISO classes.

Panel Manufacturing

Panel Manufacturing

High-grade PUF, Rockwool, and EPS double skin sandwich panels designed for air tightness and thermal efficiency.

HVAC Engineering

HVAC Engineering

Advanced Air Handling Units (AHUs), duct design, chiller integrations, and smart controls designed for pharmaceutical demands.

HVAC Validation

HVAC Validation

Accredited validation services including Air Velocity, ACH, HEPA integrity (PAO), recovery time, and non-viable particle counts.

Facility Qualification

Facility Qualification

Execution of Design Qualification (DQ), Installation (IQ), Operational (OQ), and Performance (PQ) protocols for production lines.

Documentation Services

Documentation Services

Development of SOPs, Site Master Files, validation protocols, risk assessments, and compliance packages for audits.

Engineered to Qualify

Why Choose Airzon Services?

We maintain strict adherence to environmental controls and ISO validation guidelines to deliver flawless sterile operations.

GMP Compliance

Total documentation tracing following WHO rules.

ISO Standard Setup

Designs conforming to class ISO 5, 6, 7 & 8.

Expert Engineers

Experienced validation consultants and mechanics.

End-to-End Solutions

Turnkey design, supply erection, and testing checks.

Pharma Laboratory Validation
Sectors We Support

Advanced Cleanroom Solutions By Industry

Pharmaceuticals

Pharmaceuticals

Bulk drugs formulation blocks matching US FDA Class A guidelines.

Biotechnology

Biotechnology

Genetic engineering laboratories requiring complete containment.

Hospitals & OT

Hospitals & OT

Modular positive-pressure Operating Theatres and ICU isolation modules.

Testimonials

What Our Clients Say

Ready to Discuss Your Erection & Validation Requirements?

Contact our lead engineers today to review your ISO classification goals.

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ZYDUS
NOVARTIS
CIPLA
FORTIS
DR. REDDY
ZYDUS
NOVARTIS
CIPLA
FORTIS
DR. REDDY