Pharma machinery factory in China: Settling colony count and plankton determination requirements: at the same time of each experiment, count the settling colony of microorganisms in the operating room and laminar flow table, record the results in the user log, and record the original data of the experimental environment in the experiment report. Disinfection requirements: Every week and every operation in the sterile room, the operating table and the dead corners should be wiped with appropriate disinfectant. The specific method is to use sterile gauze impregnation disinfection solution to clean the entire inner surface of the super clean bench, and aseptic room, flow of people, logistics, buffer room floor, transfer window, door handle. Cleaning and disinfection procedures should be from the inside out, from high clean areas to low clean areas. Gradually exit the clean area. Then turn on the aseptic air filter and UV lamp for 1-2h sterilization to kill the remaining microorganisms. At the end of each operation, wipe the workbench with the above disinfection solution, remove indoor moisture, and sterilize with UV lamp for 30min. Find additional details at tablet punches and dies.
The mask making machine is used to manufacture various masks with certain filtering performance by hot pressing, folding and forming, ultrasonic welding, waste cutting, ear belt and nose beam welding and other processes of multi-layer non-woven fabrics. The mask production equipment is not a single machine, but requires the cooperation of multiple machines to complete various processes. The popular mask equipment in the market include: cup type mask machine, non-woven flat mask machine, N95 mask machine, 3m9001/9002 folding mask machine, duck mouth type mask machine, three-dimensional dust-proof mask machine, etc.
The filling speed of the capsule filling machine is fast, and the size difference of the capsule filling machine is small. It integrates the powder capsule shell finishing, capsule cap finishing and capsule package, which is compact and convenient. In addition, the capsule filling machine has many advantages, such as fast arrangement speed, high efficiency, simple operation, convenient maintenance and low power consumption. It is the preferred capsule filling (filling) machine for pharmaceutical factories, health product factories, hospital preparation rooms, etc
Why is Proper Humidity Important in Clean Rooms? Maintaining proper humidity levels in clean rooms is crucial for several reasons: Prevention of Condensation: High humidity levels can cause condensation on surfaces, leading to potential damage to sensitive equipment or materials. Lower humidity levels prevent this issue by reducing water vapor in the air. Mold Growth: High relative humidity levels promote the growth of mold and mildew, which can negatively impact the cleanliness and functionality of clean rooms. Ensuring proper humidity levels helps prevent mold growth and associated health hazards.
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 tuyere equipped with filter, the auxiliary air duct can be selected according to the tuyere form, that is, the straight pipe section with the same section as the tuyere and the length equal to twice the side length of the tuyere is made of hard plate, which is connected to the outside of the filter tuyere. The measuring points are evenly arranged on the outlet plane of the auxiliary air duct according to the minimum number of measuring points, and the wind speed of each point is measured with a hot ball anemometer. The air volume is determined by multiplying the average wind speed at the section of the air outlet by the net section area of the air outlet.
A clean room is defined as a room with air filtration, distribution, optimization, construction materials and devices, where specific regular operating procedures are used to control airborne particulate concentrations to achieve an appropriate level of particulate cleanliness. 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 electricity. A specially designed room that is controlled within a certain demand range. Discover more details at https://www.sz-pharma.com/.
Quality pharma machinery manufacturer factory: 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.
The frame of the clean shed can be generally divided into three types: stainless steel square pass, varnished iron square pass and industrial aluminum profiles. The top and the top can be made of stainless steel steel plate, lacquered cold plastic steel plate, anti-static mesh curtain and acrylic plexiglass and other materials. Anti-static mesh curtains or plexiglass are generally used around, and FFU clean air supply units are used in the air supply unit.