Pharma clean room manufacturer today: It can be assembled and disassembled conveniently and quickly, realizes the general standardization of temporary buildings, and establishes the concept of environmental protection, energy saving, fast and efficient construction. The temporary housing has entered a field of stereotyped products that can be serialized development, integrated production, supporting supply, and inventory. It is used in construction sites for temporary offices, dormitories, railways, transportation, water conservancy, oil, natural gas and other large-scale field exploration and field operations construction houses; urban municipal temporary commercial or other houses; leisure villas and holiday houses in tourist areas. Discover more information at sz pharma.
Establish the use of standard operating specifications (SOP) and strict management: Items entering the clean room (aseptic room) basic requirements: All items entering the clean room (aseptic room) must be sterilized with disinfectant on the external surface in the first buffer room, and then sent to the aseptic room through the logistics buffer room, transfer window for more than 1 hour, and sterile air drying. Sterile indoor fixed items shall not be arbitrarily brought out. Personnel entering the clean room (aseptic room) requirements: experimental personnel entering the clean room (aseptic room) shall not make up, wear watches, rings and other jewelry. After cleaning your hands, you should enter the first buffer room and change your clothes. At the same time, you should change your disinfecting slippers, take off your coat, disinfect your hands with disinfectant, put on sterile gloves, change your sterile hoodie (do not expose your hair, clothes, etc.), and put on a sterile mask. Then put on a second pair of sterile gloves, and change a second pair of disinfectant isolation slippers when entering the second buffer room. Then through the air shower room 30s air shower into the sterile room.
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.
For the unidirectional flow (laminar flow) clean room, the air supply volume is determined by the product of the average wind speed of the room section and the cross-sectional area, in which the measured section of the vertical unidirectional flow (laminar flow) clean room is the horizontal section 0.8m away from the ground; The horizontal unidirectional flow (laminar flow) clean room takes a vertical section 0.5m away from the air supply surface. The spacing of measuring points on the section shall not be greater than 2m, and the number of measuring points shall not be less than 10, which shall be evenly arranged. Hot bulb anemometer for instrument.
Cleanroom pharma manufacturer with sz-pharma.com: Obstacles such as work desks in the clean room will have eddy currents at the junctions, and the cleanliness will be relatively poor near them. Drilling air return holes on the work desks will minimize eddy currents; assembly Whether the selection of materials is appropriate and whether the equipment layout is perfect are also important factors for whether the airflow becomes a vortex phenomenon. The above introduction is related to clean room and airflow influencing factors.
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.
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. Discover even more information on https://www.sz-pharma.com/.