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MODULAR CLEANROOM SYSTEMS
Custom Modular Cleanroom Systems for ISO 5–8 Controlled Environments
Design, manufacturing and installation of configurable modular cleanroom systems for pharmaceutical, medical device, biotechnology, electronics and precision manufacturing facilities.
Biogreen develops each cleanroom around the required cleanliness classification, production process, room layout, airflow strategy, temperature and humidity conditions, pressure relationships and equipment arrangement.
Equipment Integrated Into Your Cleanroom Project
Supporting contamination-control equipment can be integrated according to production flow and facility layout.
Fan Filter Unit — FFU
Ceiling-mounted filtration units providing filtered airflow to controlled cleanroom areas.
HEPA Terminal Box
Terminal filtration equipment integrated into cleanroom air-supply systems.
Air Shower
Personnel or material decontamination equipment positioned at selected cleanroom entrances.
Pass Box
Controlled material-transfer equipment designed to reduce unnecessary movement between cleanroom zones.
Laminar Airflow Unit
Localized unidirectional filtered airflow for contamination-sensitive processing areas.
Cleanroom Doors
Flush cleanroom-compatible doors available in different access, sealing and interlocking configurations.
From Cleanroom Requirement to Installed Facility
1. Requirement Assessment
We collect information about your production process, room dimensions, required cleanliness classification, environmental conditions, equipment and facility limitations.
2. Concept Design
Our engineering team develops the preliminary room zoning, personnel flow, material flow and airflow strategy.
3. Detailed Engineering
Cleanroom architecture, HVAC, filtration, utilities and equipment interfaces are coordinated before manufacturing begins.
4. Manufacturing & Preparation
Cleanroom components and supporting systems are prepared according to the approved project design.
5. Installation & Commissioning Support
The cleanroom is installed, inspected and prepared for project-specific testing, commissioning and validation activities.
Selected Cleanroom Project Experience
Pharmaceutical Production Cleanroom
Industry: Pharmaceutical Manufacturing
Scope: Cleanroom architecture, HVAC integration and supporting equipment
A controlled manufacturing environment developed around production zoning, personnel movement, material transfer and environmental-control requirements.
Medical Device Cleanroom
Industry: Medical Device Manufacturing
Scope: Modular cleanroom design and installation
A configurable cleanroom environment designed around the customer’s equipment arrangement and manufacturing workflow.
Electronics Manufacturing Cleanroom
Industry: Precision Electronics
Scope: Controlled production environment and filtration system
Designed to reduce airborne contamination where particulate control is important to manufacturing quality.
Modular Cleanroom FAQ
Modular cleanrooms can be configured for different cleanliness classifications including ISO 5, ISO 6, ISO 7 and ISO 8 depending on room design, airflow, filtration, process conditions and operational requirements.
The engineering team normally evaluates room dimensions, production process, required cleanliness classification, personnel, equipment, temperature, humidity, pressure, exhaust requirements and existing facility conditions.
Yes. Modular construction is frequently used to create controlled production areas inside existing industrial buildings, subject to structural, HVAC, utility and facility assessments.
Yes. Room dimensions, production zones, doors, windows, airlocks, material-transfer areas, equipment interfaces and supporting systems can be configured according to the manufacturing process.
Yes. HVAC can be engineered as part of the complete cleanroom project. The required configuration depends on cleanliness class, room load, temperature, humidity, pressure and manufacturing conditions.
ISO classifications define different limits for airborne particle concentrations. The correct classification should be selected according to the production process and applicable quality or regulatory requirements rather than automatically choosing a cleaner classification.
Modular construction allows future expansion or layout modification to be considered during the original engineering stage. Actual expansion feasibility depends on available facility space, HVAC capacity and the original cleanroom configuration.
Pricing depends on cleanroom area, ceiling height, cleanliness classification, wall system, HVAC, filtration, temperature and humidity control, doors, windows, electrical systems, supporting equipment and installation location. For this reason, an accurate modular cleanroom quotation should be based on actual project requirements rather than a generic price per square meter.
