The decoration and purification project of the 100,000-level purification workshop of the GMP purification workshop of medical equipment has been completed_

The purification project of the 100,000-level clean workshop of the GMP purification workshop for medical devices has been completed. I will share a few photos of the clean workshop. Let's take a look. Welcome to correct the GMP medical device purification workshop: (1) There is no obvious pollution around the factory. The factory area should be hygienic and tidy, with good greening, and try not to expose the ground. The building materials of the factory should be easy to keep clean. (2) There should be suitable and sufficient workshop area for production and quality inspection. GMP medical device purification workshop (1) There is no obvious pollution around the factory. The factory area should be hygienic and tidy, with good greening, and try not to expose the ground. The building materials of the factory should be easy to keep clean. (2) There should be suitable workshops with sufficient area for production and quality inspection, and maintain good supply of water, electricity and gas. Achieve: The production of different products in the same production area and the adjacent production area should be free from interference and pollution; various pharma machinery and materials can be arranged neatly and reasonably; the process connection should be reasonable, the flow of people and logistics should be separated, and one-way flow should be maintained. (3) According to the requirements of technology and quality, the production area is divided into clean grades, generally divided into 100 grades, 1000 grades, 10000 grades and 100000 grades, and the clean area should maintain positive pressure. The pressure difference of 4.9 Pa or more should be maintained in the interval of different cleanliness. (4) The temperature and humidity of the clean area should be adapted to its production and process requirements. The temperature is generally controlled at 18-24°C, and the relative humidity is preferably controlled at 45%-65%. (5) The water, electricity and gas transmission pipelines in the pharmaceutical cleanroom shall be located in the technical interlayer. The building surface shall be smooth, seamless, free from falling off or adsorbed dust, and suitable lighting, heating, ventilation and necessary air conditioning facilities shall be provided. .

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