Electronics Industry Clean Room Project Customized Design Supplied With Applicable CE Certified Equipment

Product Overview

A cleanroom is a controlled environment designed to limit airborne contamination and maintain specified environmental conditions. Depending on the production process, parameters such as particle concentration, temperature, humidity, pressure and electrostatic conditions can be controlled according to project requirements and applicable standards.

Cleanroom Description

Technical Reference Data

Cleanroom solutions are tailored to the cleanliness level required, the room layout, the production process and the HVAC design of each individual project.

The parameters listed below are based on specifications published by SHP. They are intended as reference configurations and not as fixed values for every cleanroom installation.

HEPA Box Reference Specification

FFU Reference Specification

Cleanroom System Configuration

Note: Final equipment selection, dimensions, airflow, filtration level and environmental control parameters are defined by the project design together with the required cleanroom classification.

Features at a Glance

• Customized cleanroom layout based on production requirements
• HVAC and HEPA filtration for controlled air cleanliness
• FFU-based air supply options
• Temperature, humidity and differential pressure control
• Cleanroom-compatible wall and ceiling systems
• Integrated electrical and lighting systems
• Cleanroom installation and commissioning
• Testing and validation support

Real World Project Case Description

Electronics Industry Cleanroom Project

Customized Cleanroom Solution for Electronics Manufacturing

Constructcn provides customized cleanroom solutions for electronics manufacturing, including cleanroom structure, HVAC systems, HEPA filtration, FFU and related cleanroom equipment.

The solution can be designed according to the customer's production process, cleanliness requirements, facility conditions and workflow.

Main Solution:

Modular cleanroom structure
HVAC and air purification
HEPA filtration and FFU
Cleanroom doors and windows
Personnel and material flow control
Installation and commissioning

Project Photos

1.SHP Engineering Team at an Electronics Cleanroom Project Site

2. completed electronics industry cleanroom interior

Engineering Process

SHP's cleanroom projects are delivered through an integrated engineering process covering design, manufacturing, installation, commissioning and performance verification.

1. Requirement Assessment

The project starts with an assessment of the customer's production process, required cleanliness classification, room functions, personnel and material flow, environmental conditions and supporting utilities.

2. Cleanroom Layout & System Design

Based on the project requirements, the engineering team develops the cleanroom layout and coordinates the enclosure structure, HVAC system, air distribution, filtration, electrical systems, doors, windows and supporting cleanroom equipment.

3. Equipment & Component Manufacturing

Cleanroom panels and related equipment are manufactured according to the approved project requirements. SHP's product range includes cleanroom panels, AHUs, FFUs, HEPA boxes, air showers, pass boxes, clean benches, cleanroom doors and windows.

4. On-Site Installation

The cleanroom enclosure, HVAC system, filtration equipment, electrical systems and supporting components are installed and coordinated on site. Wall and ceiling joints, penetrations and equipment interfaces are sealed and inspected as part of the cleanroom construction process.

5. Commissioning & System Adjustment

After installation, HVAC and filtration systems are commissioned and operating conditions are adjusted according to the project requirements. Airflow, pressure relationships and environmental parameters are checked before final testing.

6. Cleanroom Performance Testing

Applicable cleanroom performance parameters are tested according to the agreed project requirements. Testing may include airborne particle concentration, airflow, differential pressure, temperature, humidity and other environmental parameters.

7. Validation & Project Handover

Where included in the project scope, SHP can provide DQ, IQ, OQ and PQ documentation together with testing records, operation manuals, maintenance information and cleanroom drawings.

The acceptance criteria and documentation are determined according to the cleanroom classification, application and contractual project requirements.

Project Experience

1.Mauritius National Cleanroom Project – Medical Device Manufacturing

SHP has publicly documented its involvement in a national cleanroom project in Mauritius for medical appliance production and sterilization.

The project focused on establishing an ISO-certified controlled environment for medical-device-related manufacturing processes. SHP provided purification engineering solutions including HEPA filtration, environmental control for temperature and humidity, airborne particle control and cleanroom validation procedures.

Project Application: Medical Device Manufacturing

Location: Mauritius

Project Scope: Cleanroom purification system, HEPA filtration, environmental control and validation

Cleanroom Requirement: ISO-certified controlled environment

This project demonstrates SHP's experience in delivering controlled-environment solutions for contamination-sensitive medical manufacturing applications.

2.Bangladesh Electronics Cleanroom Project

SHP has also publicly documented the successful completion and handover of a cleanroom installation for an electronics manufacturer in Bangladesh.

The project was designed to meet ISO Class 7 (10,000) requirements and was developed for the production of sensitive electronic components.

Project Application: Electronics Manufacturing

Location: Bangladesh

Cleanroom Classification: ISO Class 7 (10,000)

Project Type: Electronics Manufacturing Cleanroom

The project provides a reference for cleanroom applications where airborne particle control and a stable manufacturing environment are important.

3.Romania Turnkey Cleanroom Project

In Romania, SHP completed a turnkey cleanroom project covering design, fabrication, installation and commissioning. The publicly documented project included modular cleanroom wall and ceiling panels, seamless coved epoxy flooring, ceiling-mounted FFU arrays with HEPA filtration, LED lighting and cleanroom doors with vision panels.

Following installation, SHP engineers conducted on-site inspection and cleanroom performance verification, including particle counting and airflow measurements for the FFU/HEPA filtration system.

Project Location: Romania

Application: Pharmaceutical and microbiological applications

Project Type: Turnkey Cleanroom Engineering

Scope: Design, fabrication, equipment supply, installation, commissioning and cleanroom performance verification

The project was completed and handed over after the documented inspection and validation process.

Cleanroom Testing & Verification

Cleanroom performance should be checked after installation and commissioning according to the applicable project requirements.

The cleanroom projects publicly documented by SHP include on-site inspection and performance verification of the installed systems. For the Romania turnkey project, this included inspection of wall-panel sealing, doors and windows as well as particle-count and airflow measurements for the FFU/HEPA filtration system.

Typical Verification Items

Airborne Particle Count
Airflow Measurement
Differential Pressure
Temperature
Relative Humidity
HEPA/FFU Performance
Cleanroom Enclosure Integrity
Lighting and Other Environmental Parameters Where Required

Validation Documentation

Depending on the project scope, cleanroom documentation can include:

Design Qualification (DQ)
Installation Qualification (IQ)
Operational Qualification (OQ)
Performance Qualification (PQ)
Cleanroom Test Reports
Commissioning Records
Operation and Maintenance Documentation

Testing Evidence

Where project testing documentation is available, relevant test reports and verification records can be provided as supporting project evidence.

The specific testing items, acceptance criteria and documentation depend on the cleanroom classification, the application and the agreed project requirements.

 

Related Products

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Company Profile

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Founded in 2003, SHP is engaged in cleanroom engineering and manufacturing, specializing in cleanroom systems, HVAC integration, cleanroom panels, doors and windows, FFUs, air showers and related cleanroom equipment.

 

The company delivers design, manufacturing, installation, commissioning and technical support services for pharmaceutical, biotechnology, medical device, laboratory and electronics applications. Operating under an ISO 9001:2015 quality management system, SHP supports both equipment supply and turnkey cleanroom engineering projects according to customer specifications and applicable industry requirements.

 

Drawing on more than 20 years of industry experience, SHP has participated in cleanroom projects in domestic and international markets and continues to support its customers through engineering, manufacturing and project implementation services.

 

Our Certification

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  CE Certification applies to the applicable cleanroom equipment or electrical products supplied for the project. Certification scope depends on the specific equipment and applicable EU directives/regulations.

 

Shown below are the CE certifications for the air shower, FFU, and pass box.

 

Customer Photos

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Packing and Shipping

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FAQ

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Q1: Where is your company?

A1:Our company is located in Suzhou City, close to Shanghai. It's a 1.5-hour drive from PVG Airport.

Q2: Are you a manufacturer or a trading company? What can I buy from you?
A2: We are manufacturers. We focus on cleanroom projects, air showers, FFUs, Pass boxes, dosing rooms, laminar flow hoods and benches, AHUs, and sealed doors and Windows. 

Q3:When is your delivery time? 
A3: If your cleanroom project includes AHU, the delivery time is 35 days. If you purchase goods without an AHU, the delivery time is 10 days. 

Q4: How long is your warranty period? What kind of after-sales service can you offer?
A4: Our warranty period is one year after the completion of the project. During the warranty period, if there are any problems, we will replace it. If you can't handle it, we will send an engineer to solve it for free.

Q5:Can you conduct cleanroom validation? 
A5: Yes. We can provide documentation and support for DQ, IQ, OQ and PQ, depending on the project requirements. We can also provide FAT/SAT support, equipment operation manuals, maintenance guides and a complete set of cleanroom drawings.

Q6:What are your advantages?
A6: We have a complete technical team consisting of 12 senior cleanroom and HVAC engineers to provide you with technical support. Our engineering team has completed more than 2,100 cleanroom projects in China and overseas, covering pharmaceutical, medical, laboratory, electronics and other controlled-environment applications. Such as Japan, Indonesia, Thailand, India, Saudi Arabia, Mauritius, Singapore, Australia, Canada, the United States, and others.