Clean room standard provider 2022? This specification is formulated to implement important national guidelines and rules, creating standard construction acceptance requirements, unify testing strategies, and ensure project top quality, save extra 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. See even more info at clean room class.
The clean room must be realized according to the design drawings. If the design needs to be changed during construction, there shall be a change notice from the design unit. Construction and acceptance cannot be carried out without drawings and technical requirements. Before the construction of the clean room, a detailed construction scheme and procedures shall be formulated. During the construction, all types of work shall cooperate closely and construct according to the procedures. The type of work constructed first shall not hinder the subsequent construction.
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!
The main materials, equipment, finished products and semi-finished products used in the project shall comply with the design regulations, and shall be provided with factory certificate or quality appraisal certificate. When there is doubt about the quality, it must be inspected. Expired materials shall not be used.
As long as you want the clean room project, Suzhou Pharma Machinery Co., Ltd. will realize it for you. Choose a reliable engineering company, Suzhou Pharma Machinery Co., Ltd., will be responsible for your project to the end, and the reputation is guaranteed. Our company has completed 500+ clean room projects all over the world. Many new and old customers like to buy the products they want in our company. The price is reasonable, the integrity is guaranteed, and the after-sales service is good.
During the construction of the clean room, the intermediate inspection and acceptance shall be carried out after the construction of each process, and the records shall be put on record. In addition to this specification, the construction and acceptance of the clean room shall also comply with the provisions of the current relevant national standards.The architectural decoration construction of the clean room shall be carried out after the completion of the roof waterproof works and the external enclosure structure, the installation of the external doors and windows, and the acceptance of the main structure.
The detection of air volume and wind speed must be carried out first, and all effects of purified air conditioning must be obtained under the designed air volume and wind speed. Before air volume detection, it is necessary to check whether the fan operates normally, whether all components in the system are installed correctly and whether there are obstacles (such as whether the filter is blocked or blocked). All valves should be fixed at a certain opening position, and the size of the measured air outlet and air duct must be measured. For the turbulent flow clean room, the air supply volume shall be determined by the air outlet method or air duct method. See Item 6, 7 and 8 respectively. For the air outlet without filter, the method in Appendix I of the current national standard code for construction and acceptance of ventilation and air conditioning engineering (gbj243) can be implemented.
Its contents include the indoor decoration works, the installation of doors and windows, the gap sealing, as well as the sealing of the joints between various pipelines, lighting lamps, purification Suzhou Pharma is one of the leading turnkey project providers for pharmaceutical, food, herbal, cosmetic, electronics factory and chemical plants. We offer projects as per GMP regulations. As being pioneers in this field, the solutions from Suzhou Pharma is readily accepted by the customers.
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.
Many single-flow type clean rooms are designed as vertical laminar flow, so the uniformity of wind speed is very important. Only uniform vertical laminar flow can effectively eliminate particulate pollution. For non-single-flow type clean rooms, since the concept of particle control is dilution, not immediate elimination, generally speaking, the air exchange rate is far more important than the wind speed, so it is only necessary to measure the air volume. See extra information on sz-pharma.com.