ISO Standard Modular Clean Room Turnkey Project Professional Supplier
Suzhou Pharma Machinery is a set design, production, sales, installation services as one of the high-end purification equipment enterprises. The products produced by Suzhou Pharma include dust-free workshop, laboratories, hospitals and other construction equipment materials, purification equipment, purification filters, stainless steel products, purification engineering supporting products and other series.
The clean workshop is also called the dust free workshop,the clean room(Clean Room) and the dust free room.
It refers to the removal of pollutants such as particles,harmful air and bacteria in the air within a certain space,
and the indoor temperature,cleanliness,indoor pressure,air velocity and air distribution,noise and vibration,lighting
and static control.A specially designed room for a particular requirement.That is to say,
no matter how the external air conditions change,the room can maintain
the characteristics of cleanliness,temperature and humidity and pressure.
Cleanliness |
Class 100 to Class 100000, ISO 5 to ISO 8, Class B to Class D |
Project include |
1. Structure: Wall Panel, Ceiling Panel, Windows, Doors, Various Fittings, Flooring |
2.Electric: Lighting, Switch, Cables, Wires, Power Distribution Cabinet, etc |
3.HVAC: AHU, Ducting, Piping, Chiller, dehumidifier, etc. |
4.Auto-control: PLC Controller, Sensors for Humidity and Temperature, Control Panel |
5. Process Piping System: Gas, Water Pipeline |
Temperature&Humidity |
As clients request |
Application |
Pharmaceutical Industry |
Qualification Documents |
IQ, OQ, PQ,DQ |
Our Service |
Professional Consultation, User-friendly English Sofaware, 24 hours technical support,Foreign installation and commissioning |
In a pharmaceutical production packaging cleanroom designated as ISO 8, rigorous controls are in place to minimize
the 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 strict
gowning procedures, limiting access, and regularly monitoring and testing the environment for particle counts and
microbiological contaminants. Despite being less stringent than some other cleanroom classifications, an ISO 8 cleanroom
still plays a vital role in preventing contamination that could compromise the efficacy or shelf life of pharmaceuticals.