Full Turnkey Dust Free Cleanroom Construction Modular One Stop Service

Product Overview 

Cleanrooms are controlled environments designed for high-precision industries, helping reduce airborne particulate matter and microbial contamination within enclosed areas. Equipped with professional air handling units, FFU systems, and HEPA filtration, cleanroom systems can support the control of indoor temperature, humidity, and air circulation according to defined project requirements.

Cleanrooms are widely used in semiconductor manufacturing, pharmaceutical processing, biotechnology, hospitals, laboratories, and other applications where controlled hygiene and cleanliness conditions are required. Our services cover the full cleanroom engineering process, including design, construction, system integration, performance testing, commissioning, and after-sales technical support.

Each solution can be configured according to customer requirements, site layout, production processes, required cleanliness classification, and applicable industry regulations. Cleanroom systems are inspected and tested according to the specified project requirements and applicable cleanliness classification. This approach supports reliable, energy-conscious, and maintainable cleanroom operation for industrial production, laboratory, and research applications worldwide.

Cleanroom Description

Technical Specifications

Final specifications are determined according to the cleanroom classification, production process and project requirements.

Features at a Glance

• Maintains the required level of air cleanliness through high-efficiency HEPA filtration, helping remove airborne dust, fine particles, and microorganisms.
• Provides adjustable control of indoor temperature, humidity, and differential pressure to support a stable and controlled working environment.
• Uses a sealed cleanroom structure to help limit external pollution and reduce the risk of cross-contamination between different functional zones.
• Applies engineered airflow design and balanced air circulation to support consistent cleanliness performance throughout the controlled space.
• Supports low-particle and controlled environments for pharmaceutical, electronics, medical device, and research laboratory applications where contamination control is required.
• Helps control bacterial and microbial contamination through appropriate environmental control measures, with cleanroom configurations designed according to applicable GMP requirements and international cleanliness classifications.
• Features a well-sealed, thermally insulated structure to help reduce the impact of external weather and environmental changes on the controlled production area.
• Can be equipped with energy-efficient air handling systems for automated environmental adjustment and reliable long-term operation.
• Supports customized cleanliness levels, layout plans, and system configurations according to different industrial processes and site conditions.
• Uses easy-to-clean and antibacterial materials to support routine disinfection, maintenance, and ongoing cleanroom operation.
  

Cleanroom Applications

Pharmaceutical & Biotechnology

Modular cleanroom systems can be configured for pharmaceutical and biotechnology applications requiring controlled airborne contamination, environmental conditions and pressure relationships.

Laboratory & R&D

Prefabricated cleanrooms can be adapted for laboratory, testing and research environments according to the required cleanliness classification and process conditions.

Electronics & Semiconductor

Cleanroom configurations can support electronics and precision manufacturing processes where airborne particle and environmental control are important.

Medical & Healthcare

Cleanroom systems can be configured for selected medical, healthcare and controlled production environments according to applicable project requirements.

Integrated Cleanroom System Components

Complete Cleanroom Material and Equipment Supply

In addition to cleanroom engineering services, SHP supplies the partition-type cleanroom panels, built-in filtration frames, HVAC systems and cleanroom doors essential to turnkey cleanroom project delivery.

The following illustration presents the core systems and products supplied within SHP cleanroom projects.

Mauritius Project

Pharmaceutical Cleanroom Project – Mauritius

Project Overview

In Mauritius, SHP completed a turnkey pharmaceutical cleanroom project including design, manufacturing, HVAC installation, commissioning and final validation.

Project Information

Project Challenges

The project required a GMP-compliant production environment with strict control of airborne particles, temperature, humidity and differential pressure to support pharmaceutical production.

SHP Solution

• Modular cleanroom panel system
• Air handling unit (AHU) system
• HEPA filtration system
• Environmental monitoring system
• Pressure control system

Cleanroom Construction Progress Record

Cleanroom Panel Delivery and Material Preparation

Cleanroom wall and ceiling panels were delivered to the project site and organized according to the installation schedule. All materials were inspected before installation to ensure compliance with project specifications and cleanroom construction requirements.

 

HVAC Ductwork Fabrication and Installation

The HVAC installation team carried out on-site ductwork fabrication and assembly for the cleanroom ventilation system. Proper duct routing and sealing are essential for maintaining airflow uniformity, pressure control and contamination prevention.

 

Cleanroom Ceiling Grid and Utility Framework Installation

The ceiling suspension system and utility support framework were installed to accommodate cleanroom panels, lighting fixtures, HEPA filtration units and process utilities. This stage forms the structural foundation for the final cleanroom enclosure.

 

 

Project Completion

 

Cleanroom installation completed according to the project scope.
HVAC installation and commissioning completed.
Cleanroom performance testing conducted.
Validation and project acceptance completed according to the documented project requirements.

 

AVB Testing Report

 

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Third-Party Performance Testing & Validation

Independent testing and validation were conducted after project completion to verify cleanroom performance and environmental control effectiveness.

Validation Services

• Design Qualification (DQ)
• Installation Qualification (IQ)
• Operational Qualification (OQ)
• Performance Qualification (PQ)

Testing Items

• Airborne Particle Count Test
• Airflow Velocity Test
• Differential Pressure Test
• Temperature Test
• Humidity Test
• Illumination Test
• Noise Test

Third-Party Verification

The cleanroom system was tested and documented by an independent testing organization to verify compliance with project specifications and applicable cleanroom standards.