Solution

Cosmetics industry

Electronic industry

Biopharmaceutical industry

Chemical Industry

Refrigeration industry

Food Industry

Laboratory

Office decoration

Biopharmaceutical industry

The goal of GMP required by biopharmaceutical enterprises is to ensure the establishment of a scientific and strict sterile drug production environment, process, operation and management system, to eliminate all possible and potential biological activity, dust and pyrogen pollution to the maximum extent, and to produce high-quality, hygienic and safe drug products. What we call biopharmaceutical purification engineering-GMP clean workshop engineering solutions and pollution control technology is one of the main means to ensure the successful implementation of GMP;
Through in-depth research on the production environment of biopharmaceutical customers and accumulation of engineering experience, we clearly understand the key to environmental control in the biopharmaceutical production process. Energy saving is the priority of our system plan. What we are best at is to give customers environmental solutions that meet the requirements of GMP and Fed 209D,ISO1464,IEST and EN1822 international standards and apply the latest energy-saving technologies; we can provide the whole plant planning and design from GMP-people flow and logistics purification scheme, clean air conditioning system and clean decoration system. The whole plant energy-saving renovation, water and electricity, ultra-pure gas pipelines, clean room monitoring, maintenance systems and other comprehensive installation and supporting services.

Cosmetics industry

Cosmetics industry

In the design and equipment of the plant, it is required to exclude dust, bacteria and other pollutants in the air within a certain space range, and control the temperature, humidity, airflow and static electricity of the workshop within a certain range, so that there are purification standards such as 100000 level and 300000 level. According to the "Cosmetic Production License Work Standard" issued by the State Food and Drug Administration after the "Two Certificates in One", manufacturers need to submit a test report that can prove that the production environment conditions meet the requirements in order to obtain the new meal "Cosmetic Production License". It is specifically pointed out that for the production of eye skin care cosmetics, skin care cosmetics for infants and children, the air cleanliness in the filling room and cleaning container storage room during the production period should meet the 300000 requirements.

Electronic industry

Electronic industry

The definition of the microelectronics purification project is to exclude the dust particles, harmful air, bacteria and other pollutants in the air within a certain space range, and to control the indoor temperature and humidity, cleanliness, indoor pressure, airflow velocity and airflow distribution, noise vibration and lighting, static electricity within a certain range of demand, and to give a specially designed confined space. Optical microelectronics purification project, also known as clean room or clean room, is now an indispensable important facility in semiconductor, precision manufacturing, liquid crystal manufacturing, optical manufacturing, circuit board manufacturing and biochemistry, medicine, food manufacturing and other industries. In recent years, due to the innovation and development of technology, the demand for high precision and fine miniaturization of products is more urgent, such as the research and manufacture of super-large volume circuits, which has become a project that countries all over the world attach great importance to in the development of science and technology, and our company's design concept and construction technology are in a leading position in the industry.

Biopharmaceutical industry

Biopharmaceutical industry

The goal of GMP required by biopharmaceutical enterprises is to ensure the establishment of a scientific and strict sterile drug production environment, process, operation and management system, to eliminate all possible and potential biological activity, dust and pyrogen pollution to the maximum extent, and to produce high-quality, hygienic and safe drug products. What we call biopharmaceutical purification engineering-GMP clean workshop engineering solutions and pollution control technology is one of the main means to ensure the successful implementation of GMP; Through in-depth research on the production environment of biopharmaceutical customers and accumulation of engineering experience, we clearly understand the key to environmental control in the biopharmaceutical production process. Energy saving is the priority of our system plan. What we are best at is to give customers environmental solutions that meet the requirements of GMP and Fed 209D,ISO1464,IEST and EN1822 international standards and apply the latest energy-saving technologies; we can provide the whole plant planning and design from GMP-people flow and logistics purification scheme, clean air conditioning system and clean decoration system. The whole plant energy-saving renovation, water and electricity, ultra-pure gas pipelines, clean room monitoring, maintenance systems and other comprehensive installation and supporting services.

Chemical Industry

Chemical Industry

The selection principle of the plane type of chemical plant is to make it as simple as possible to meet the requirements of the production process, strive to beautify, and at the same time follow the requirements of the building regulations. The plant type used in chemical design is generally rectangular, T-shaped, L-shaped and II, etc. Rectangle is convenient for the layout of the general plan, saves land, helps to arrange equipment, shortens pipelines, is easy to arrange traffic entrances and exits, and has more walls for natural lighting and ventilation. However, sometimes due to the long total length of the factory building, when the general plan layout is difficult, in order to meet the requirements of terrain or production, L-shaped, T-shaped or I II-shaped are also used, at this time, the factors of lighting, ventilation, passage and facade should be fully considered.

Refrigeration industry

Refrigeration industry

The weight of the refrigerator in the refrigeration room and the refrigeration and cooling water pumps matched with the refrigerator are large, and the vibration and noise during operation are also large. They are usually arranged on the bottom of the building or the basement. If it is a high-rise building with group rooms, the refrigeration room should be arranged in the basement of the podium building, and noise elimination and vibration isolation should be done, especially the vibration reduction of the water pump amount freezing and cooling water pipe supports and hangers. The adjacent and upper rooms of the refrigeration room should be places where the requirements for noise attenuation and vibration isolation are not high. Refrigeration room should be set up to send, exhaust equipment, in order to remove indoor waste heat in time, add fresh air. The temperature in the machine room shall be ≤ 36 ℃. Noise elimination measures shall be taken in the machine room to prevent the operation noise of the unit from transmitting to the air-conditioned room or affecting the outdoor environment. Artificial lighting shall be provided in the machine room, and sufficient illumination shall be provided around the control switches and operation instruments.

Food Industry

Food Industry

The food/beverage aseptic clean workshop is best isolated from the outside world and cannot be disturbed by walking or other factors. The size of the food/beverage aseptic clean workshop depends on the needs and is generally composed of a dressing room, a buffer room, an air shower room and an operation room. The dressing room is located outside, mainly for changing clothes, hats, shoes, etc. The buffer room is located between the dressing room and the air shower room, and can also be used for several operation room phrases at the same time. The operation room is located in the inner room, mainly for product grouting. The room should not be exposed to direct sunlight. It should be suitable for large and small shops (the height of the specific simulation production equipment is determined). Room Et is large, please sweep and consumption inconvenience; Too small, inconvenient to operate; Too high quality will affect the effective fruit of the first penny. Enhancement should be improved without dead corners, so as to make cleaning and disinfection. Food and beverage should be closed and the static pressure difference of the vehicle net should be kept at positive pressure. UV lamps, air filter purifiers and constant temperature devices for air disinfection should be set up.

Laboratory

Laboratory

Laboratories are mainly used in microbiology, biomedicine, biochemistry, animal experiments, gene recombination and biological products, collectively referred to as clean laboratories-biosafety laboratories. The biosafety laboratory consists of the main functional laboratory, other laboratories and auxiliary functional rooms. Biosafety laboratories must ensure personal safety, environmental safety, waste safety and sample safety, and can operate safely for a long time. At the same time, they also need to provide a comfortable and good working environment for laboratory staff.

Office decoration

Office decoration

The clean room for plant decoration must be constructed according to the design drawings, and the design needs to be modified during construction shall be notified by the design unit. No drawings and technical requirements can not be construction and acceptance. Clean room building decoration construction schedule arrangement should be with other professional types of work to develop a clear construction cooperation plan, according to the procedure of construction, cooperate with each other. The architectural decoration construction of clean room shall be carried out after the completion of roof waterproofing works and outer enclosure structure, the installation of outer doors and windows and the acceptance of the main structure. The contents include interior decoration works, installation of doors and windows, gap sealing, and sealing operations of gaps at the combination of various pipelines, lighting lamps, purification air conditioning equipment, process equipment and other parts with the building. Elastic sealing materials and dustproof coatings used for caulking in clean rooms must be provided with instructions indicating the composition, variety, delivery date, storage validity period and construction method, as well as product qualification certificates. Expired products and unidentified products shall not be used.

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