GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical

Product Details
Customization: Available
Certification: CE, ISO9001
Noise: 60-70db
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Number of Employees
108
Year of Establishment
2004-03-10
  • GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical
  • GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical
  • GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical
  • GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical
  • GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical
  • GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical
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  • Overview
  • Product Description
  • Technical Features
  • Product Parameters
  • Company Profile
  • Certifications
  • Exhibition
  • Packaging & Shipping
Overview

Basic Info.

Model NO.
ISO 1/4/5/8
Application
Pharmacy Clean Room
Control Mode
Button
Usage
Dust Removal, Smoke Removal, Sterilization
Clean Grade
Class a
Transport Package
Wooden Case
Specification
customized
Trademark
HJ CLEAN TECH
Origin
China
Production Capacity
10000/Year

Packaging & Delivery

Package Size
250.00cm * 2500.00cm * 250.00cm
Package Gross Weight
500.000kg

Product Description

Product Description

GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical
A cleanroom is a specialized space designed with professional techniques to control pollutants such as dust and microorganisms
in the air at extremely low concentrations,
while strictly regulating environmental parameters like temperature, humidity, pressure, and air flow.
Its core objective is to provide a clean and stable environment for high-precision production, scientific research, and experiments, preventing pollutants from affecting product quality or experimental results.

Technical Features

GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical

1. High-Precision Cleanliness Control

Air Filtration System: Through multi-stage filtration by primary, medium, high-efficiency (HEPA), or ultra-high-efficiency (ULPA) filters, airborne particles (such as dust, bacteria, viruses, etc.) are removed. Cleanliness levels can reach ISO 1 to ISO 9 (or Federal Standard 209E Class 1 to Class 100,000), meeting the needs of different industries (e.g., ISO 1 for semiconductor manufacturing and ISO 5 for pharmaceutical production).
Airflow Organization Design: Unidirectional flow (vertical or horizontal), non-unidirectional flow (turbulent), or mixed flow patterns are adopted. Reasonable supply and return air layouts ensure uniform air movement, reducing eddies and pollutant accumulation.

2. Precise Regulation of Environmental Parameters

Temperature and Humidity Control: Equipped with a constant temperature and humidity air conditioning system, the temperature deviation is typically controlled within ±0.5ºC~±2ºC, and humidity deviation within ±2%~±5%. This prevents fluctuations from affecting precision equipment operation or production processes (e.g., chip manufacturing is extremely sensitive to temperature and humidity).
Pressure Control: By adjusting pressure differences (usually maintaining 5~10Pa positive or negative pressure), it prevents external pollutants from invading or internal pollutants from spreading, suitable for isolation between different clean areas (e.g., various process zones in pharmaceutical workshops).
GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical
GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical

3. Special Requirements for Materials and Structure

Walls and Floors: Made of dust-resistant, corrosion-resistant, and easy-to-clean materials (such as stainless steel, epoxy resin coatings, PVC panels), with smooth and seamless surfaces to reduce dust adhesion and microbial growth.
Sealing Design: Parts like doors, windows, and pipeline interfaces are sealed to prevent external polluted air from penetrating and internal airflow from leaking.

Product Parameters

Cleanless Number of particles ≥0.1μm / cubic meter Number of particles ≥0.5μm / cubic meter
ISO 1 10 0.35
ISO 4 10,000 350
ISO 5 100,000 3,500
ISO 8 100,000,000 350,000

Company Profile

GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical
GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical
GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical
GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical

SUZHOU HJCLEAN TECH CO., LTD was established in 2004 in Suzhou,jiangsu Province, The company's headquarters is located in Suzhou industrial Park, and production bases have been established inSuzhou and jingjiang. Branches are set up in Wuhan, chengdu, Xi'an, jinan and Shenyang across the country,The company has been focusing on the research, development, production, sales and customized services of aseptic ultra-clean equipment, testing instruments and cleanroom engineering.
It mainly produce equipments and instruments of clean room deals in business of clean room proiects for pharmaceutical factory, laboratory, medical organization etc...
The company has more than 50 patents products, ISO9001 certification and CE certification. The company is a member of china clean room association and is one of jiangsu Engineering Technology Research Center. We are in a leading position in the field of clean room.The company's products including sterility isolator, negative pressure isolator ,vhp pass box,vhp generator, atomized sterilizer , bag in bag out filter system , suspended particle online monitoring system, airborne particle counter, air sampler, airborne bacterial counter, air flow capture hood,aerosol generator and photometer, glove integrity tester, dispensing booth, laminar air flow hood,purified cart trolley, laminar air flow cabinet , biosafety cabinet, static pass box, dynamic pass box, air shower etc have been sold to countries around the world from the establishment to the present.
The company boasts a professional team comprisind R&D specialists, desian enaineers, and seasonedtechnicians, supported by state-of-the-art testing equipment and precision manufacturing systemsWith lean management svstems alianed with lSO standards, we deliver products that excel in both premium quality and exceptional cost-effectiveness.
Guided by our core tenets of Customer-first Philosophy, Technological Leadership, Service Excellence and Pioneering Innovation, we are dedicated to delivering integrity-driven partnerships for globally benchmarked enterprises.

Certifications

GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical

Exhibition

GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical

Packaging & Shipping

GMP Standard ISO 7 Design and Installation Modular Clean Room for Pharmaceutical

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