Pharmaceutical cleanroom manufacturer 2022

Excellent clean room class factory by SZ-pharma? This specification is created to implement important national guidelines and policies, unify construction acceptance requirements, unify testing methods, and ensure project top quality, save extra energy, protect 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. Read additional info on pharmaceutical cleanroom.

The clean room must be built according to the design plans. If the design needs to be modified 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.

Mainly control the pollution of air dust particles and organisms (bacteria) to working objects, and maintain a negative pressure with the atmosphere inside. Pharma cleanroom project It is suitable for precision machinery industry, electronics industry, aerospace industry, high-purity chemical industry, atomic energy industry, optomagnetic product industry, LCD, computer hard disk; pharmaceutical industry, hospital, operating room, sterile ward, food, cosmetics, beverage products Animal laboratory, physical and chemical laboratory, blood station, etc. More cases check our cleanroom project page.

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.

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.

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.

The clean room is generally made of foam color steel or rock wool board with a vertical wall and an independent air-conditioning air supply system. The air is filtered through high-efficiency three-stage filtration in junior high schools. The personnel and materials are equipped with an air shower room and a transfer window for clean filtration.

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. See even more details at https://www.sz-pharma.com/.

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