Turn-key project for clean room wholesale provider 2024: 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. See extra details at gmp panel.
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.
Labeller is a device that pastes rolled self-adhesive paper labels (paper or metal foil) onto PCB, products or specified packaging. It has a wide range of applications, and can meet the full circle labeling or semi circle labeling of round bottles. The labeling switching between bottles is simple and easy to adjust. Blister packaging machine is a machine that uses transparent plastic film or sheet to form a blister and seals the product between the blister and the bottom plate by means of heat sealing and bonding. Application: capsule, plain tablet, sugar coating, capsule, injection, abnormity, etc., as well as sealed packaging of medical devices, light food, electronic components blister.
Efficiency of Equipment: Some equipment, such as electronics and mechanical components, require specific humidity levels to function correctly. Maintaining the right humidity levels in clean rooms ensures optimal performance and longevity of these critical pieces of equipment. How to Maintain Optimal Humidity Levels in Clean Rooms? To maintain optimal humidity levels in clean rooms, consider the following steps: Install a Dehumidifier: A dehumidifier is an essential tool for maintaining proper humidity levels in clean rooms. It removes excess moisture from the air, keeping humidity levels within the desired range. Choose a dehumidifier based on the size of your clean room and the relative humidity requirements you need to meet.
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.
Pill stamp press supplier with SZ-pharma: Generally, the air flow distribution point on the surface of the operating table or production equipment should be located at 2/3 of the distance between the clean room space and the partition wall, so that when the operator is working, the air flow can flow from the inside of the process area to the operation area, and the The dust is taken away; if the distribution point is arranged in front of the process area, it will become an improper airflow distribution. At this time, most of the air flow will flow to the process area, and the dust caused by the operator’s operation will be brought to the back of the equipment. As a result, the platform will be polluted, and the yield rate is bound to decrease.
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. Read even more information at https://www.sz-pharma.com/.