Pill stamp press manufacturer and supplier in China: 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. Discover more details at cleanroom pharma.
Tablet press is mainly used for tablet technology research in pharmaceutical industry. The tablet pressing machine presses powder or granular raw materials into tablets. Its scope of application: Traditional Chinese medicine, western medicine, health products, food, chemical industry, electronics and other industries. The prefabricated container house is a new concept of environmentally friendly and economical house with light steel H-shaped steel and channel steel as the framework, sandwich panel as the wallboard material, space combination with standard modulus series, and bolted or welded components.
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.
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.
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.
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.
With our vast experience in handing national and international Pharma/Laboratory Projects.we ensure that professional integration of project will have plenty of benefits. The company has complete infrastructure and a team of experienced personnel to managing these fields more professionally. When it comes to your cleanroom certification,we have the qualifications and experience to deliver a comprehensive validation service off facilities to he requirements of all the current standard and guidelines globally.And our cleanroom are CE Market to show they meet the requirements of local country directives. Discover more details on sz-pharma.com.
Excellent tablet press dies manufacturer: 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.
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 control is within a certain demand range, and a specially designed room is given. That is to say, no matter how the external air conditions change, the interior can maintain the characteristics of cleanliness, temperature, humidity and pressure that were originally set. The main function of the clean room is to control the cleanliness and temperature and humidity of the atmosphere that the product comes into contact with, so that the product can be produced and manufactured in a good environmental space. We call such a space a clean room.