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Integrated One Stop Production Service For General Industrial Cleanroom Projects
| Brand Name: | SHP |
| Model Number: | Customized |
| MOQ: | 50 square meters |
| Price: | $500.00/square meters 50-499 square meters |
| Payment Terms: | L/C,T/T |
| Supply Ability: | ≥1 set |
industrial cleanroom project service
,general cleanroom production solutions
,one-stop cleanroom construction service
Integrated one-stop production service for general industrial cleanroom projects
Product Overview
SHP delivers turnkey cleanroom solutions for general industrial applications, integrating engineering design, equipment manufacturing, on-site installation, commissioning and validation into a single project delivery process.
With 20+ years of cleanroom engineering experience and 2,100+ completed projects across 40+ countries, SHP helps manufacturers create controlled production environments that meet ISO 14644 and GMP standards. Our cleanrooms utilize HEPA filtration, advanced HVAC systems and modular cleanroom structures to ensure stable environmental control, contamination prevention and long-term operational reliability.
Mauritius Project
Pharmaceutical Cleanroom Project – Mauritius
Project Overview
SHP successfully completed a turnkey pharmaceutical cleanroom project in Mauritius, providing design, manufacturing, HVAC installation, commissioning and validation services for the customer.
Project Information
| Item | Details |
| Location | Mauritius |
| Industry | Pharmaceutical Manufacturing |
| Solution | Turnkey Cleanroom Project |
| Scope | Design, HVAC, Installation, Validation |
| Cleanroom Class | ISO 7 |
| Status | Successfully Delivered |
Project Challenges
The customer required a GMP-compliant production environment with strict control of airborne particles, temperature, humidity and differential pressure to support pharmaceutical manufacturing operations.
SHP Solution
- Modular cleanroom panel system
- Air handling unit (AHU) system
- HEPA filtration system
- Environmental monitoring system
- Pressure control system
Project Construction Progress
The following photos show actual construction activities carried out during the Mauritius pharmaceutical cleanroom project.
Image 1:HVAC Duct Insulation Installation
HVAC Ductwork Insulation Installation – Pharmaceutical Cleanroom Project
Project engineers performed on-site installation of HVAC duct insulation materials to improve thermal efficiency and maintain stable temperature and humidity control within the cleanroom environment.
The insulation system was installed according to the approved HVAC design specifications and cleanroom engineering requirements.
Image 2:Cleanroom Panel Measurement
On-site Measurement and Cleanroom Panel Layout Verification
Before installation, project engineers conducted field measurements and panel layout verification to ensure accurate fitting of cleanroom wall and ceiling panels.
This step helps reduce installation deviations and ensures compliance with cleanroom construction tolerances and project design drawings.
Image 3:Client Site Inspection
Client Inspection During Cleanroom Installation
The client visited the project site during the installation stage to review construction progress and verify compliance with project requirements.
Regular communication between the engineering team and project stakeholders helps ensure smooth project execution and successful delivery.
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
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
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
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
Cleanroom Description
| Application | Pharmaceutical | Lab | Electronics |
| Cleanliness | Class 100–100000 or applicable ISO/GMP classification | ISO 5–8 or project-specific classification | ISO 5–8 or project-specific classification |
| Scope |
Structure part; Partition and ceiling panel; door and window,epoxy. |
HVAC part; AHU and chiller; Ducting and piping. |
Electrical part; Lamp,switch and socket; Distribution cabinet. |
| Service | Design and production | Construction and test | Validation and training |
| Wall/ceiling panel | Machine-made or Hand-made sandwich board |
| Clean room equipment | Air shower,FFU,Pass box,Laminar flow cabinet,hepa box |
| Cleanliness | Class 100-100000 |
| Purification system | HVAC, or AC conditioner+FFU |
| Floor | PVC anti-static floor or epoxy-based coating |
| Other addessores | stalinite window,LED panel light,Door,Hand wash sink,storage/shoe cabinet etc |
| Service | Design,manufacturing,construction |
Cleanroom Core Functions
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Contamination ControlFilter airborne dust, particles and microbes to avoid cross-contamination and pollution-caused product faults.
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Stable Indoor ClimatePrecisely manage temp, humidity and air pressure to avoid material deformation, oxidation and static.
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Boost Product Qualification RateUltra-clean surroundings lower scrap rate, stabilize batch quality and raise production yield.
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Protect Precision MachineryReduce dust adhesion on devices, minimize abrasion & precision drift and cut maintenance cost.
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Ensure Operator SafetyPositive pressure design keeps hazardous pollutants out to protect workshop staff.
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Meet Global Industry StandardsConform to ISO14644, satisfying audit requirements for electronics, medical, food & optics industries.
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Anti-static & Risk ControlBalance humidity to eliminate static, protect sensitive parts and prevent potential fire hazards.
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.
Relevant Cleanroom Project Experience
Mauritius Turnkey Pharmaceutical Cleanroom Project
Location: Mauritius
Application Industry: Pharmaceutical Manufacturing
Project Category: Turnkey Cleanroom Project
Cleanroom Class: ISO 7
Delivered Scope: Design, HVAC, Installation and Validation
Status: Successfully Delivered
Cleanroom Testing & Validation
To confirm performance, cleanroom testing is carried out according to the project requirements and applicable standards. Depending on the system configuration, this may include airborne particle counting, airflow velocity, differential pressure, temperature, humidity, illumination, noise and filter integrity testing where applicable.
SHP can support project qualification documentation, including DQ, IQ, OQ and PQ where required.
