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China, Chinese CE Certification Medical Clean Rooms ISO7 Cleanroom1 Industrial Products Supplier Manufacturer Details, price list catalog:
China Industrial Products Supplier Manufacturer List Catalog
Air Clean EquipmentAir ShowerGMP Clean RoomModular Clean Room
Suzhou Pharma Machinery Co., Ltd.
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Product Description What is ISO Standard cleanroom?The ISO standard specifies the cleanliness of clean rooms. Air cleanliness refers to the degree of the number of dust particles in the air in a clean environment. The level of air cleanliness is the most important parameter standard for clean rooms, and it is an important basis for determining whether clean rooms are qualified. The smaller the number of the ISO level name, the higher the cleanliness. So you can see IS01 has the highest cleanliness and IS09 has the lowest cleanliness. ISO standard cleanroom is often used to evaluate the semiconductor, bio-pharmaceutical, laboratory and research, new energy and other fields of clean room, dust-free room or aseptic room environment; and different industries have different requirements for cleanliness level. CleanlinessClass 100 to Class 100000, ISO 5 to ISO 8, Class B to Class DProject include1. Structure: Wall Panel, Ceiling Panel, Windows, Doors, Various Fittings, Flooring2.Electric: Lighting, Switch, Cables, Wires, Power Distribution Cabinet, etc3.HVAC: AHU, Ducting, Piping, Chiller, dehumidifier, etc.4.Auto-control: PLC Controller, Sensors for Humidity and Temperature, Control Panel5. Process Piping System: Gas, Water PipelineTemperature&HumidityAs clients request ApplicationPharmaceutical IndustryQualification Documents IQ, OQ, PQ,DQOur ServiceProfessional Consultation, User-friendly English Sofaware, 24 hours technical support,Foreign installation and commissioningIn a pharmaceutical production packaging cleanroom designated as ISO 8, rigorous controls are in place to minimizethe introduction and spread of contaminants, ensuring the integrity and safety of the packaged pharmaceutical products.This includes controlling air flow, using High-Efficiency Particulate Air (HEPA) filtration systems, maintaining strictgowning procedures, limiting access, and regularly monitoring and testing the environment for particle counts andmicrobiological contaminants. Despite being less stringent than some other cleanroom classifications, an ISO 8 cleanroomstill plays a vital role in preventing contamination that could compromise the efficacy or shelf life of pharmaceuticals.If you want clean room for your Pharmaceutical or Related factory/Hospital/Electric product factory/Plant growing green house...etc,You need provide these basic information to us:1.What size clean room do you want to build?Do you have layout drawing?2.What temperature and humidity do you want for your clean room?Whats local temperature and humidity?3.What product or work will be do in the clean room?4.Do you have factory now or just ground?5.Whether have other special requirement?Please note and let me know these information,it will help us more clear your idea.Best regardsMia
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