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1904 Tower Plaza, Sheikh Zayed Road, opp. The Future Museum, Dubai, UAE

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business@hawklandglobalfz.com

Services / Cleanroom & HVAC Engineering

Cleanroom & HVAC Engineering

Controlled environments that protect your product and pass your audits.

From a single sampling booth to a full sterile manufacturing suite, Hawkland Global designs, supplies and validates cleanrooms and HVAC systems that meet international GMP standards.

Overview

Clean Air Is the Foundation of Quality

In pharmaceutical manufacturing, the room is part of the process. Air cleanliness, pressure cascades, temperature and humidity all affect product quality and regulatory approval. A poorly designed HVAC system can cause cross-contamination, failed batches and audit findings that are expensive to fix.

Hawkland Global takes a complete approach. We design the room layout and HVAC system together, supply modular cleanroom panels, doors and air-handling equipment, and validate the finished installation against ISO 14644 and EU GMP grade requirements.

Our Cleanroom & HVAC Services

Cleanroom Design

Zoning, personnel and material flow, airlock design and pressure cascades for Grade A to D and ISO 5 to ISO 8 areas.

Modular Cleanroom Panels

Wall and ceiling panel systems, flush glazing, coved corners and epoxy or vinyl flooring built for easy cleaning.

Pharmaceutical HVAC

Air handling units, HEPA terminal filters, ductwork, chillers and dehumidification sized for your room classifications.

Controlled Equipment

Laminar airflow units, pass boxes, dispensing booths, sampling booths, air showers and biosafety cabinets.

Monitoring & BMS

Building management and environmental monitoring systems that record pressure, temperature, humidity and particle counts.

Testing & Certification

HEPA integrity testing, airflow velocity and air-change checks, particle counting, recovery tests and smoke studies.

Areas We Engineer

Sterile Areas
Aseptic filling rooms, Grade A/B zones, RABS and isolator surroundings
Oral Solid Dosage
Dispensing, granulation, compression, coating and capsule areas with dust control
Liquids & IV Plants
Solution preparation, filling and container-forming areas for LVP and SVP production
Quality Control Labs
Microbiology labs, sterility testing suites and instrument rooms
Warehousing
Temperature-controlled stores, sampling areas and cold rooms
Utilities
Purified water and WFI plant rooms, compressed air and technical areas

From Concept to Certification

01

Site Survey & URS

We assess the building and define a user requirement specification with your quality team.

02

Basic & Detailed Design

Layouts, HVAC zoning, airflow calculations, P&IDs and equipment schedules ready for approval.

03

Supply & Fabrication

Panels, doors, AHUs, filters and controls are manufactured and shipped to your site.

04

Installation

Our supervisors oversee construction, ductwork, electrical and controls integration.

05

Validation & Handover

Complete DQ, IQ, OQ and PQ with test reports, as-built drawings and maintenance manuals.

Why Choose Hawkland Global

Process-Led Design

We design the room around your process and equipment, so the HVAC and layout work together from day one.

Energy-Efficient Systems

Right-sized air handling and smart controls reduce running costs without compromising classification.

Audit-Ready Documentation

Every project includes the drawings, test data and protocols that inspectors expect to see.

Single Responsibility

Design, supply, installation and validation under one contract reduce risk and save time.

Standards We Design To

  • ✓ISO 14644-1 and 14644-2
  • ✓EU GMP Annex 1 Grades A to D
  • ✓WHO GMP guidelines for HVAC systems
  • ✓ISPE Baseline Guides
  • ✓ASHRAE design standards
  • ✓EN 1822 HEPA filter classification

Industries We Serve

  • ✓Pharmaceutical and biotech plants
  • ✓IV fluid and parenteral facilities
  • ✓Hospital pharmacies and compounding units
  • ✓Medical device manufacturing
  • ✓Food and nutraceutical processing
  • ✓Research and QC laboratories

Integrated with Your Production Line

On turnkey IV/LVP projects, Hawkland Global delivers the cleanroom and HVAC package alongside the process machinery. This keeps room classification, equipment layout and utilities aligned from the first drawing.

View Case Studies

Frequently Asked Questions

Can you upgrade an existing facility?

Yes. We assess existing rooms and HVAC systems, identify gaps against current GMP requirements and plan upgrades that keep disruption to a minimum.

Which cleanroom grades can you design?

We design areas from ISO 8 / Grade D up to ISO 5 / Grade A, including aseptic processing zones.

Do you provide validation and recertification?

We provide initial validation at handover and can support periodic requalification, including filter integrity and particle count testing.

How long does a cleanroom project take?

Timelines depend on size and complexity. A clear schedule is agreed during the design stage, and we track it through to handover.

Build a Cleanroom That Passes First Time

Share your layout or process requirements, and our engineers will propose a compliant, energy-efficient solution.

Book a Site Survey