ISO Standard Cleanroom Project Professional Design and Installation Supplier

• After-sales Service: Online Technology Support
• Usage: Dust-Proof Workshop, Electrostatic Workshop, Food And Chemical Industry, Warehouse, Pharmaceutical Factory
• Window: Double Layer Window
• Shipping Cost: Estimated freight per unit.: about shipping cost and estimated delivery time.
• Currency: US$
• Return&refunds: You can apply for a refund up to 30 days after receipt of the products.
• Model NO.: SZP
• Clean Grade: ISO7
• Size: Custom Design
• Floor: PVC Floor
• HVAC System: Temperature&Humidity
• Lighting: LED Light
• Application: Industrial
• Door: Single/Double Swing Door
• Product Name: Cleanroom
• Type: Modular Design
• Cleanroom Height: 3-5m or Customized
• Design Software: CAD
• Temperature/Humidity Control: Customized Design
• Changing Room: Male/Female
• Laboratory: Custom Design
• Transport Package: 20 Feet Containers
• Specification: Custom Request
• Trademark: PHARMA
• Origin: China
• HS Code: 8414809090
• Production Capacity: 2000 Square Meters /Year
• Package Size: 100.00cm * 100.00cm * 100.00cm
• Package Gross Weight: 100.000kg

Product Description

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.

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

Clean room is a special designed room to exclude the particles in the air, bacteria and other harmful air pollutants, and the
indoor temperature, cleanliness, interior pressure, air velocity and air distribution, noise, vibration, and lighting, static
control within the scope of a certain demand. That is no matter how the outside air conditions change, its indoor all can
maintain the original set requirements of cleanliness, temperature and humidity and pressure performance characteristic.

The main function of clean room is to control the cleanliness and temperature & humidity of the atmosphere that products
(such as silicon) contact, can make the products in a good environment of production and manufacturing, this space we
call it clean room. According to international practice, dust-free purification level mainly be decided according to the
number of air particle diameter per cubic meter is greater than the standard number of particles. That is the so-called no dust,
is not 100% no dust, but control on a very tiny amounts of units. Of course accord with standard of dust particles in the standard
relative to our common dust is very small, but for optical structure, even just a bit of dust will have a very negative impact,
so on the optical structure of production, no dust is the inevitable requirement.

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.