1904 Tower Plaza, Sheikh Zayed Road, opp. The Future Museum, Dubai, UAE
business@hawklandglobalfz.com
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.
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.

Zoning, personnel and material flow, airlock design and pressure cascades for Grade A to D and ISO 5 to ISO 8 areas.
Wall and ceiling panel systems, flush glazing, coved corners and epoxy or vinyl flooring built for easy cleaning.
Air handling units, HEPA terminal filters, ductwork, chillers and dehumidification sized for your room classifications.
Laminar airflow units, pass boxes, dispensing booths, sampling booths, air showers and biosafety cabinets.
Building management and environmental monitoring systems that record pressure, temperature, humidity and particle counts.
HEPA integrity testing, airflow velocity and air-change checks, particle counting, recovery tests and smoke studies.
We assess the building and define a user requirement specification with your quality team.
Layouts, HVAC zoning, airflow calculations, P&IDs and equipment schedules ready for approval.
Panels, doors, AHUs, filters and controls are manufactured and shipped to your site.
Our supervisors oversee construction, ductwork, electrical and controls integration.
Complete DQ, IQ, OQ and PQ with test reports, as-built drawings and maintenance manuals.
We design the room around your process and equipment, so the HVAC and layout work together from day one.
Right-sized air handling and smart controls reduce running costs without compromising classification.
Every project includes the drawings, test data and protocols that inspectors expect to see.
Design, supply, installation and validation under one contract reduce risk and save time.
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 StudiesYes. We assess existing rooms and HVAC systems, identify gaps against current GMP requirements and plan upgrades that keep disruption to a minimum.
We design areas from ISO 8 / Grade D up to ISO 5 / Grade A, including aseptic processing zones.
We provide initial validation at handover and can support periodic requalification, including filter integrity and particle count testing.
Timelines depend on size and complexity. A clear schedule is agreed during the design stage, and we track it through to handover.
Share your layout or process requirements, and our engineers will propose a compliant, energy-efficient solution.
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