Premium iso5 cleanroom factory in China? In order to maintain the required temperature, humidity, wind speed, pressure and cleanliness in the clean room, the most commonly used method is to continuously send a certain amount of treated air into the room to eliminate various heat and humidity interference and dust pollution in the clean room. To obtain the air in a certain state into the clean room, a whole set of equipment is needed to process the air, and it is continuously sent into the room, and part of it is continuously discharged from the room. This whole set of equipment constitutes a clean air conditioning system. Read additional information on https://www.sz-pharma.com/iso5-iso8-cleanroom.html.

Clean air-conditioning system is to control outdoor substances that affect the clean environment of clean rooms, such as dust, smoke, microorganisms, etc. It is a very important part in medical and health, food processing, and microelectronics engineering.

The clean air conditioning system is basically composed of the following equipment:

1. Heating or cooling, humidification or dehumidification and purification equipment;
2. Air conveying equipment and pipelines that send the treated air into each clean room and circulate it;
3. Provide heat, cold, heat source, cold source and piping system to the system.

This specification is formulated to implement relevant national guidelines and rules, creating standard construction acceptance requirements, unify testing strategies, and ensure project high quality, save more energy, shield the environment and safe operation during the construction of clean rooms (including prefabricated clean rooms, the same below). This specification is applicable to the construction and acceptance of newly-built and reconstructed industrial clean rooms and general biological clean rooms, and is not applicable to the construction and acceptance of special biological clean rooms with biological safety requirements.

Cleanroom workshop take the control of inanimate particles as the object. Mainly control the pollution of the living objects with living particles to the outside situation and people. The negative pressure inside the atmosphere must be maintained. it’s suitable for bacteriology, biology, clean laboratory, physical engineering, recombinant genes, vaccine preparation. In order to know your requirement, please fill the following table carefully and supply CAD layout, so that we can provide correct scheme and quotation, thank you!

In Africa, some area only require cooling system of the air conditioning unit. Especially at island country, the air humidity is very higher 80-90% of year average. For noodles, pasta production factory, the humidity should be control at 30-40%. Like this condition we recommend rotary dehumidifier air conditioner or independent dehumidifier with air conditioner work together.

For the unidirectional flow (laminar flow) clean room, the air supply volume is determined by the product of the average wind speed of the room section and the cross-sectional area, in which the measured section of the vertical unidirectional flow (laminar flow) clean room is the horizontal section 0.8m away from the ground; The horizontal unidirectional flow (laminar flow) clean room takes a vertical section 0.5m away from the air supply surface. The spacing of measuring points on the section shall not be greater than 2m, and the number of measuring points shall not be less than 10, which shall be evenly arranged. Hot bulb anemometer for instrument.

Today (Suzhou Pharma Machinery Co., Ltd.) will introduce to you, clean room airflow and influencing factors. There are many factors affecting the airflow in the clean room, such as process equipment, personnel, clean room assembly materials, lighting fixtures, etc. At the same time, the distribution point of airflow above the production equipment should also be considered.

Suzhou Pharma engaged in cleanroom turnkey project for many years, HVAC system design and installation is the main part in project. We supply air duct design, AHU solution and installation guide. Before we quote the equipment, the basic data is necessary, such as room clean grade, dimension and height, temperature and humidity request, the local highest/lowest temperature and humidity.

A clean room refers to the removal of particulates, harmful air, bacteria and other pollutants in the air within a certain space, and the indoor temperature, cleanliness, indoor pressure, airflow speed and airflow distribution, noise vibration and lighting, Static control is within a certain demand range, and a specially designed room is given. That is to say, no matter how the external air conditions change, the interior can maintain the characteristics of cleanliness, temperature, humidity and pressure that were originally set. The main function of the clean room is to control the cleanliness and temperature and humidity of the atmosphere that the product comes into contact with, so that the product can be produced and manufactured in a good environmental space. We call such a space a clean room.

With our vast experience in handing national and international Pharma/Laboratory Projects.we ensure that professional integration of project will have plenty of benefits. The company has complete infrastructure and a team of experienced personnel to managing these fields more professionally. When it comes to your cleanroom certification,we have the qualifications and experience to deliver a comprehensive validation service off facilities to he requirements of all the current standard and guidelines globally.And our cleanroom are CE Market to show they meet the requirements of local country directives. Discover additional information on https://www.sz-pharma.com/.

Governments of various countries have different requirements for clean design conditions, so attention should be paid to government requirements when designing. The choice of refrigerant should pay attention to whether it needs environmental protection type.

The cleanroom advantage include:

1. handmade sandwich panels can always be customized to meet every need,module width, module height are variable dimensions. no need cutout in the Installation site.
2. GMP double layer glass walls can customized.They allow to see into the production process and create a different working atmosphere.
3. LED lights reach UL standard.
4. For special hygiene requirements, our offers higher-quality integrated,hollow-profiles systems that prevent ingress of dire,air dust and moisture. Our design according to ISO14644-1 International standard.
Suzhou Pharma hope that in this new year, we have a new breakthrough in clean room technology, which can help more friends in need.