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Focuses On Professional Cleanroom Project And Pharmaceutical Cleanroom Equipment.

Clean workshop project acceptance

Clean workshop project acceptance

The inspection of clean workshop engineering acceptance and routine inspection should be empty or static, and the inspection and monitoring of use acceptance should be dynamic. When necessary, the inspection can also be determined through negotiation between the construction party, the construction party and the inspection party state. The wind system is a hidden project, and the general clean workshop project...

Text label: clean pharmaceutical cleanroom acceptance, clean engineering acceptance, clean workshop engineering

Clean workshop project acceptance

The inspection of clean workshop engineering acceptance and routine inspection should be empty or static, and the inspection and monitoring of use acceptance should be dynamic. When necessary, the inspection can also be determined through negotiation between the construction party, the construction party and the inspection party state. The air system is a hidden project. After the interior of the general clean workshop project is completed, it is difficult to adjust the quality of the air system. In order to ensure that the indoor environment required by the project can meet the standards and meet the needs of users, the air system needs to be divided. project acceptance; the thickness, combustion performance and corrosion resistance of the air duct and its thermal insulation materials shall meet the requirements of fire protection regulations; the air duct shall be provided with pre-buried pipes or protective casings, pre-buried pipes or protective sleeves when passing through walls and fire zones. The wall thickness of the pipe steel plate should not be less than 1.6mm, the gap between the air duct and the casing should be sealed with non-combustible flexible materials that are harmless to human health, then sealed with sealant, and finally the surface is decorated.

The length dimension of the inner side of the frame opening for installing the high-efficiency filter shall not be positive deviation, and the allowable negative deviation shall not be greater than 3mm; the frame for installing the high-efficiency filter shall not be flat, and the allowable deviation of the flatness of the installation frame of each high-efficiency filter shall It is 1mm; after the high-efficiency filter is installed and before the comprehensive performance measurement, it is not suitable to install the diffuser plate and decorative layer; the high-efficiency filter for sending and exhausting the air is used for the purpose of filtering biological aerosols, and it is a clean workshop of grade 5 or above or Air supply end high-efficiency filters with special requirements should be scanned on-site one by one to detect leaks, and should be qualified. For clean rooms below level 5 whose main purpose is to filter non-biological aerosols, air supply high-efficiency filters or their end devices are installed. On-site scanning should be carried out to detect leaks, and the leak detection ratio should not be lower than 25%; the resistance of the high-efficiency filter installed in each independent clean environment should be reasonably adjusted. Between the filters, the difference between the rated resistance of each set and the average value of the rated resistance of each set should be less than 5%. During the acceptance process, the actual measured value of the high-efficiency filter product should be checked; about the number of tests, according to the order for installing multiple filters. 20% of the number of air inlets or air supply surfaces shall be sampled, but not less than one air supply outlet or air supply surface; for the dynamic air flow sealed return and air outlet high-efficiency filter devices with differential pressure gauges, the air supply shall be sent to Wind pressure test, the reading of the differential pressure gauge should be above 10Pa, and all air outlets with differential pressure gauge should be checked during the test and observation. Zhongjing Global Purification can provide consulting, planning, design, construction, installation, transformation and other supporting services for clean workshops and clean projects.

The test items that should be adjusted during the operation confirmation during the completion acceptance include: detection of the rotation number, air volume and outlet static pressure of the fan; measurement and balance of the air volume of the system and each room; detection and adjustment of the static pressure difference between the same rooms; Adjustment system linkage operation, precise setting and adjustment; temperature and humidity setting and adjustment; scanning leak detection of all high-efficiency filter installation frames and filter element bodies; indoor air cleanliness level; switching inspection of different operating conditions specified in the design. The contents that need to be tested for the performance acceptance of clean pharmaceutical cleanroom or clean area include: air cleanliness test, planktonic bacteria and sedimentation bacteria concentration test should be carried out in biological clean workshop; static pressure difference test; wind speed or air volume test.

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Our mission is to operate the best specialty retail business in domestic, regardless of the product we sell. Because the product we sell is CUSTOM SOLUTION SERVICES, our aspirations must be consistent with the promise and the ideals of the volumes which line our manufacture.

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