Laboratory layout design of cosmetic purification workshop
layout design of cosmetic purification workshop
Cosmetics manufacturers should determine the required testing items and frequencies according to their product structure, materials used, process control requirements and product testing requirements, and allocate enough testing personnel, equipment and places according to the workload; laboratories should choose In a clean and quiet place...
Text label: Cosmetic pharmaceutical cleanroom laboratory, clean room laboratory, layout design
layout design of cosmetic purification pharmaceutical cleanroom
Cosmetics manufacturers should determine the required testing items and frequencies according to their product structure, materials used, process control requirements and product testing requirements, and allocate enough testing personnel, equipment and places according to the workload; laboratories should choose In a clean and quiet place with enough light to facilitate work, and keep a certain distance from the production and processing workshop, this arrangement can not only prevent cross-contamination, but also facilitate sampling and inspection. The laboratory includes a physical and chemical laboratory and a microbiological laboratory; the physical and chemical laboratory mainly conducts various qualitative and quantitative physical and chemical indicators, such as appearance, color, content, odor, specific gravity, viscosity, PH value, heavy metal content, etc.; instrument room Place some valuable instruments, such as gas chromatography, liquid chromatography, etc., the instrument is of high value, and requires certain specialized skills and strict operating conditions to ensure the accuracy of the test results, and needs to be managed and operated by special personnel; the testing room is for ordinary inspection work Common instruments such as pH meters, viscometers, titrators, etc. are usually placed in the place. Some standard reagents and test solutions prepared by enterprises are usually configured and stored in this area.
Cosmetic purification workshop supporting microbiological laboratory is a place dedicated to testing the microbiological level of materials and products. Generally, it can be divided into a clean area and a general area; the general area is an area for preparing and serving samples for testing. Usually, the receiving and Activities such as storage, storage and configuration of culture medium, cleaning and disinfection of testing vessels can be arranged in this area, and enterprises with conditions can also separate the above activities in different rooms to reduce mutual influence; the microbiology laboratory should also be equipped with culture To meet the needs of daily operations, enterprises should also be equipped with uninterruptible power supplies to prevent sudden power outages from affecting places that require continuous control conditions such as incubators or refrigerators. The clean area is mainly for the detection of sample microorganisms. Since the inspection process cannot be polluted and disturbed by the environment, the clean area must meet some specific requirements. For example, some enterprises stipulate that the air quality level should be controlled at level 100. This level of air purification system can be achieved by using facilities such as biological safety cabinets or ultra-clean benches; in order to ensure that the area is not polluted by the external environment, the area should be physically isolated from other areas and isolated from the ventilation system. The area goes through the buffer room and requires a second change of clothes, etc. Zhongjing Global Purification can provide consulting, planning, design, construction, installation, transformation and other supporting services for purification workshops and dust-free workshops.
Whether it is a microbiology laboratory or a physical and chemical pharma machinery, the enterprise should ensure that the laboratory has the corresponding inspection capabilities, such as whether the personnel and experimental equipment can meet the inspection accuracy and environmental requirements specified by the inspection method; The weighing accuracy is to three decimal places. If the balance configured by the enterprise can only read one decimal place, it cannot meet the inspection ability; for example, some inspection methods require the room temperature to be kept at about 25 degrees Celsius, and the ambient temperature should be strictly recorded during inspection. If the company does not install air conditioning in the laboratory, it will not be able to meet the requirements in extreme weather conditions. In order to ensure that the inspection instruments are always in good condition, enterprises should establish a management system for laboratory instruments and equipment, including the regulations and procedures for instrument calibration, instrument use methods or operating procedures, instrument cleaning or disinfection, instrument maintenance regulations and operations. The instrument should be clearly marked, and the instrument after calibration should be clearly marked with the current calibration time and the next calibration time, so as to facilitate the user to identify at any time.
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