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Hangzhou Zeda Instrument Co., Ltd

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    sale@zjuee.com

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    13372416330

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    12th Floor, Building 3, No. 1418-50 Moganshan Road, Gongshu District, Hangzhou City, Zhejiang Province

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The Quality Control Department of Qingfeng Pharmaceutical has officially launched the Zeda Instrument Temperature and Humidity Monitoring System
Date: 2023-07-06Read: 1

After half a month of construction, installation, and debugging, the Quality Control Department of Qingfeng Pharmaceutical officially launched the Zeda Instrument Temperature and Humidity Monitoring System on July 1st. The construction content of this project includes continuous temperature monitoring and alarm systems for refrigerators, incubators and other box types in the quality control department, as well as a complete set of computerized system verification services.




Qingfeng Pharmaceutical


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Qingfeng Pharmaceutical Group Co., Ltd. is an innovative pharmaceutical enterprise group that integrates drug research and development, production, and sales. The company's development strategy is driven by research and development, and has built collaborative and efficient chemical innovation drug platforms, high-value generic drug platforms, innovative natural drug platforms, and pilot conversion platforms in Shanghai, Beijing, Hangzhou, Ganzhou, and other placesWe have formed a global and full chain innovative research and development system, with nearly 60 new drug varieties under development and multiple innovative drugs undergoing clinical research in the United States.


Ze Da Instrument



Ze Da Instrument is committed to promoting our self-developed and self-produced EMS system products in the Chinese GMP industry, striving to enable Chinese pharmaceutical companies to use Chinese "smart" manufacturing.


The EaseFactor environmental monitoring system from Ze Da includes various environmental sensors (temperature, humidity, pressure difference, gas, dust particle counters, etc.) as well as supporting relays and base stations. The software complies with GMP regulations and the product has passed FDA certification, meeting the requirements of electronic signature and audit tracking in 21 CFR Part 11. We also provide professional installation implementation and post service (including third-party CNAS calibration). Our professional engineering team completes 3Q/4Q verification and computerized system verification, which can be personalized according to user templates.