Pill stamp press manufacturer 2024: The Importance of Clean Rooms: Clean rooms are designed to minimize the presence of dust, bacteria, viruses, and other contaminants that could affect product quality or pose health hazards to workers. By controlling factors such as temperature, humidity, air circulation, and cleaning methods, clean rooms help ensure that products manufactured within these environments meet strict regulatory requirements and are safe for use by consumers. The International Organization for Standardization (ISO) has developed a series of standards that outline the requirements for clean room design, construction, operation, and maintenance. The most commonly used ISO code for clean rooms is ISO 14644-1: 2015, which specifies the general layout and requirements for cleanroom facilities intended for use with biological samples. This standard covers various aspects of clean room design, including the selection of materials, installation of equipment, and management of environmental factors. Read even more details at pharma clean room.
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.
Because of the different standards and machine styles, the die of tablet press can be divided into single tablet press die and rotary tablet press die. According to different specifications, diameter and tablet shape, the stamping dies of single stamping tablet machine and rotary tablet press can be divided into circular stamping dies and special-shaped stamping dies (triangle, oval, key type, plum blossom, rectangle, etc.), which can be customized according to your needs.
In summary, maintaining the right humidity level in clean rooms is vital for ensuring their effectiveness and longevity. By understanding the normal humidity range for clean rooms (between 40% and 60% RH) and implementing proper cleanroom humidity control techniques such as using a dehumidifier, hygrometer, proper ventilation, and controlling water sources, professionals can help create a controlled environment that promotes optimal performance and safety.
Mainly control the pollution of air dust particles and organisms (bacteria) to working objects, and maintain a negative pressure with the atmosphere inside. Pharma cleanroom project It is suitable for precision machinery industry, electronics industry, aerospace industry, high-purity chemical industry, atomic energy industry, optomagnetic product industry, LCD, computer hard disk; pharmaceutical industry, hospital, operating room, sterile ward, food, cosmetics, beverage products Animal laboratory, physical and chemical laboratory, blood station, etc. More cases check our cleanroom project page.
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.
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 at https://www.sz-pharma.com/.
Top pharma clean room manufacturer factory: As long as you want the clean room project, Suzhou Pharma Machinery Co., Ltd. will realize it for you. Choose a reliable engineering company, Suzhou Pharma Machinery Co., Ltd., will be responsible for your project to the end, and the reputation is guaranteed. Our company has completed 500+ clean room projects all over the world. Many new and old customers like to buy the products they want in our company. The price is reasonable, the integrity is guaranteed, and the after-sales service is good.
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.
