99.995% HVAC Sandwich Panel Modular Clean Room 1000 Dust Free For Pharmaceutical Electronics

Product Overview 

SHP provides Class 100–100,000 modular cleanroom solutions for pharmaceutical, electronics, laboratory and medical manufacturing facilities.

With more than 20 years of cleanroom engineering experience and over 2,100 completed projects in 40+ countries, SHP delivers integrated cleanroom construction services including HVAC installation, cleanroom panel systems, HEPA filtration, commissioning and validation.

All cleanroom systems are designed according to ISO 14644 and GMP requirements to ensure stable environmental control, contamination prevention and long-term operational reliability.

Cleanroom Description

Features at a Glance

1. 1. Contaminant Prevention & Elimination
      Primary mechanism: Controlled dilution and displacement.
      Execution: HEPA/ULPA filtration coupled with laminar (unidirectional) or turbulent (mixed) airflow regimes.
      Outcome: Continuous removal and suppression of both viable (microbial) and non-viable (particulate) contamination.

   2. Environmental Process Stabilization
      Primary mechanism: Precision regulation of thermodynamic and physical variables.
      Execution: Real-time control of temperature, humidity, pressurization, and, when required, vibration and static dissipation.
      Outcome: Creation of a predictable, repeatable process foundation, negating ambient environmental drift.

   3. Spatial Containment & Risk Mitigation
      Primary mechanism: Differential energy fields (air pressure gradients) and physical segregation.
      Execution: Cascading pressure differentials (positive/negative), sealed construction, and dedicated airlocks.
      Outcome: Isolation of critical processes, prevention of cross-contamination, and containment of hazardous materials or pathogens.

   4. Protocol-Driven Human-Factor Engineering
      Primary mechanism: Standardization and proceduralization of all interactions with the controlled environment.
      Execution: Comprehensive gowning systems, material decontamination procedures, behavioral training, and defined workflows for personnel, materials, and waste.
      Outcome: Mitigation of the single largest contamination vector: human activity.

   5. Compliance-as-a-Function: Verification & Assurance
      Primary mechanism: Data-driven performance validation.
      Execution: In-situ particle counting, continuous environmental monitoring (pressure, temp/RH), and rigorous certification against standards (ISO 14644, GMP Annex 1).
      Outcome: Objective, documented proof of environmental integrity for regulatory adherence and quality assurance.

Project Case – Pharmaceutical Cleanroom Construction Project

Project Overview

Project Background

The client required a GMP-compliant pharmaceutical production facility with controlled temperature, humidity, and air cleanliness levels. SHP was responsible for the cleanroom construction, HVAC system installation, air handling equipment integration, and on-site project management.

The project included cleanroom wall and ceiling systems, air duct installation, AHU deployment, electrical routing, lighting systems, and final commissioning.

Construction Progress

Phase 1 – HVAC Equipment Installation

Installation of suspended air handling units (AHUs) and HVAC duct systems above the cleanroom production areas.

Work Completed

• AHU positioning and suspension
• HVAC duct installation
• Airflow distribution planning
• Ceiling service coordination

Engineering Highlights

• Optimized airflow routing
• Reduced pressure loss
• Easy maintenance access
• Compliance with cleanroom airflow requirements

Phase 2 – Cleanroom Wall and Ceiling Framework Installation

Installation of cleanroom panel systems and ceiling grid structures during the construction phase.

 

Work Completed

• Modular cleanroom wall installation
• Ceiling suspension system assembly
• Utility routing preparation
• Structural alignment verification

Engineering Highlights

• Modular design for rapid construction
• Smooth cleanroom surface finish
• Easy future expansion
• Improved contamination control

Phase 3 – Cleanroom Room Formation

Assembly of cleanroom enclosure structures and integration of HVAC air supply systems.

 

Work Completed

• Sandwich panel installation
• Room partition construction
• Air supply duct integration
• Equipment room preparation

Engineering Highlights

• Airtight cleanroom envelope
• Efficient airflow circulation
• GMP-oriented layout
• Flexible process room configuration

Key Systems Supplied

• Cleanroom Sandwich Panels
• Air Handling Units (AHU)
• HVAC Duct System
• HEPA Filtration System
• Cleanroom Lighting
• Electrical Distribution System
• Cleanroom Doors and Windows

Project Outcome

The cleanroom construction was completed according to the project schedule. The HVAC and cleanroom systems were successfully integrated, providing a controlled environment suitable for pharmaceutical manufacturing operations.

 

Project Features

✔ Modular Cleanroom Construction

✔ HVAC System Integration

✔ GMP-Oriented Design

✔ High Airtightness Performance

✔ Easy Maintenance Layout

✔ Turnkey Engineering Solution

 

AVB Testing Report

 

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Third-Party Performance Testing & Validation

To verify cleanroom performance and environmental control effectiveness, independent testing and validation were conducted after project completion.

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.

 

Certifications

 

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SHP operates under a certified quality management system and manufactures cleanroom equipment in accordance with international standards for quality, safety and performance. Our engineering and manufacturing processes are continuously audited to ensure compliance with global cleanroom and HVAC project requirements.

 

 

Quality Management System

 

SHP is certified to ISO 9001:2015 Quality Management System standards, covering the design, manufacturing and installation of cleanroom systems, sandwich panels and air purification equipment.

 

Certificate: ISO 9001:2015 Quality Management System Certification

 

 

CE Certification for Cleanroom Equipment

 

To support international projects and regulatory compliance, major cleanroom equipment supplied by SHP has been assessed for conformity with applicable European directives related to electrical safety and electromagnetic compatibility.

 

CE Certified Equipment Includes:

 

Air Shower Room
Fan Filter Unit (FFU)
Pass Box

 

CE Certification for Air Shower Room

 

 

CE Certification for Fan Filter Unit (FFU)

 

 

CE Certification for Pass Box

 

Commitment to Quality and Compliance

 

Through certified manufacturing processes, documented quality control procedures and project validation services, SHP ensures that every cleanroom and HVAC solution is delivered in accordance with customer specifications, GMP requirements and international cleanroom standards.

 

Applicable Standards

ISO 14644 Cleanroom Standards
ISO 9001:2015 Quality Management System
EU Low Voltage Directive (2014/35/EU)
EU Electromagnetic Compatibility Directive (2014/30/EU)
GMP Guidelines for Pharmaceutical Manufacturing
EN1886 Air Handling Unit Standard

 

Company Profile

 

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About SHP Cleanroom Engineering

SHP is a professional cleanroom engineering company specializing in the design, manufacturing, installation and validation of cleanroom systems for pharmaceutical, biotechnology, medical device, laboratory and electronics industries.

With over 20 years of industry experience, SHP provides complete turnkey cleanroom solutions from concept design to project delivery.

Company Strength

Item	Data
Industry Experience	20+ Years
Completed Projects	2100+
Countries Served	40+
Senior Engineers	12
Quality Certification	ISO 9001:2015

Core Products

• Cleanroom Turnkey Projects
• Air Handling Units (AHUs)
• Fan Filter Units (FFUs)
• Air Showers
• Pass Boxes
• Cleanroom Panels
• Cleanroom Doors & Windows

Engineering Services

• Design & Consulting
• Manufacturing
• Installation
• Commissioning
• Validation (DQ / IQ / OQ / PQ)
• After-Sales Support

Frequently Asked Questions

 

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1. What cleanroom classifications can SHP provide?

SHP designs and builds cleanroom systems ranging from ISO Class 5 to ISO Class 8, with configurations tailored to pharmaceutical, electronics, laboratory, and medical manufacturing applications. All solutions are designed according to applicable ISO 14644 and GMP requirements.

 

2. Does SHP provide complete turnkey cleanroom projects?

Yes. SHP provides turnkey cleanroom engineering services including cleanroom design, HVAC systems, cleanroom panels, electrical systems, equipment installation, commissioning, validation, and after-sales support.

 

3. How do you verify that the cleanroom meets project requirements?

After installation, cleanroom performance can be verified through particle count testing, airflow testing, differential pressure testing, temperature and humidity testing, and other validation procedures. DQ, IQ, OQ, and PQ documentation can also be provided when required.

 

4. Do you provide third-party testing or validation reports?

Yes. Independent testing organizations can conduct performance testing and validation to verify compliance with project specifications and applicable cleanroom standards.

 

5. What experience does SHP have in cleanroom engineering?

SHP has more than 20 years of cleanroom engineering experience, has completed over 2,100 projects, and has served customers in more than 40 countries worldwide.

 

6. What certifications and standards support your cleanroom projects?

SHP operates under an ISO 9001:2015 Quality Management System and supplies CE-certified cleanroom equipment for international projects. Cleanroom solutions are developed in accordance with ISO 14644, GMP guidelines, and other applicable industry standards.