Gmp panel supplier with SZ-pharma: Regular replacement of new UV lamps, replacement of the purification system of the initial effect, medium effect, high efficiency head: regular (at least once a year) replacement of new UV lamps to ensure that UV lamp sterilization continues to be effective. At least once every 2 years, or according to the cleanliness to verify the actual situation, regularly replace the initial effect, medium effect, high efficiency head. To ensure that the function of the purification system continues to be effective, and at the same time, make a replacement record in the use of the log, and regularly archive and save. During use, the movement or activity of personnel should be reduced as much as possible. Read additional information at clean room sandwich panel.
Common pharmaceutical equipment includes dryer, grinder, vibrating screen, slicer, tablet press machine, soft capsule production equipment, capsule filling machine, blister packaging machine, granule powder packaging machine, mixer, falling film evaporator, supercritical CO2 extraction machine, centrifuge,etc. The air circulation in the clean room is purified, and the return air is sent to the fan filter unit (including high efficiency/ultra-high efficiency filter, chemical filter, etc.) through the elevated floor and the return air tunnel, and then sent to the clean room for re-filtration. The overall purification process is active, forced and continuous circulation, so as to achieve the purpose of maintaining the high degree of cleanliness of the clean room air.
Pharmaceutical equipment includes: granulating oven, boiling dryer, wet machine, pulverizer, vibrating screen, slicer, drug frying machine, drug frying machine, tablet press, pill making machine, multi-functional extraction tank, liquid storage tank, liquid distribution tank, decompression drying oven, tilting reaction pot, capsule filling machine, bubble type packaging machine, particle packaging machine, powder packaging machine, V-type mixer, lifting feeder, etc.
What is the Normal Humidity for Clean Rooms? The ideal humidity level for clean rooms depends on various factors, including the type of equipment being used, the materials involved, and the specific application of the clean room. However, a general rule of thumb is that the cleanroom humidity level should be between 40% and 60% relative humidity (RH). This range provides adequate moisture levels to prevent static buildup while preventing excessive condensation that could lead to mold growth or damage to equipment.
The plane and space design of the clean laboratory will arrange the clean experimental area and personnel purification, equipment and material purification and other auxiliary rooms in different areas. At the same time, the comprehensive coordination effects of various technical facilities, such as experimental operation, process equipment installation and maintenance, air distribution type, pipeline layout and purified air conditioning system, are considered.
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.
Premium clean room in pharmaceutical industry manufacturer and supplier: 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.
Clean shed, also known as clean work shed (dust-free shed, purification shed, operating table, etc.), is a small space surrounded by anti-static mesh curtains or plexiglass in the clean room, and HEPA and FFU air supply units are used above. It is composed of a space with a higher purification level than the clean room, and the clean room can be equipped with purification equipment such as air shower room and transfer window.
What is the purpose of the clean room test of the clean workshop? Most of the owners are based on the original vision of the purification project to complete the test indicators. Of course, this is the most straightforward goal and method. After all, our intention to build a clean room is also As such, there is a need to achieve our air cleanliness. In a single-flow type clean room, the location of the wind speed measurement can be specified by the owner, usually on the surface of the filter screen or at the working height. However, it should be noted that it is the air velocity measurement of the filter screen (the surface of the filter screen) or the indoor air velocity measurement of the clean room (working height). Clean workshop, clean room, clean room — the purpose of clean workshop and clean room test. Discover extra info at sz-pharma.com.
Air filter refers to the air filter device, which is generally used in clean workshop, clean workshop, laboratory and clean room, or used for dust prevention of electronic machinery communication equipment. There are primary filter, medium efficiency filter, high efficiency filter and sub high efficiency model. Different models have different standards and performance. The comprehensive performance test of clean room includes: Wind speed, air volume (ventilation frequency), temperature and relative humidity, suspended particle number, planktonic bacteria, settling bacteria, static pressure difference, illumination, noise, air flow pattern, self purification time, high-efficiency filter leak detection, total bacterial colonies in the air, total bacterial colonies on the surface of the worktable, total bacterial colonies on the surface of the worktable, total bacterial colonies on the surface of workers’ hands, etc.