Pharmaceutical event, Su Xin Environment participates in the 91st China International Pharmaceutical Raw Materials/Intermediates/Packaging/Equipment Trade Fair

Publication Date:2024-10-25 Author: Sothis Environmental
From October 16th to 18th, the 91st China International Pharmaceutical Raw Materials/Intermediates/Packaging/Equipment Fair (API China) was successfully held in Xi'an. Various pharmaceutical and equipment companies attended for technical exchanges and product sharing, and communicated and answered many technical issues and difficulties in the industry. SuXin Environment also showcased its products at the conference, bringing the latest generation of clean technology achievements to everyone. And delivered a speech at the forum "2024 Pharmaceutical Enterprise QC Laboratory Compliance and Management Capability Enhancement" seminar, discussing how clean room testing can assist in drug quality management.

  
On October 17th, the "2024 Pharmaceutical Enterprise QC Laboratory Compliance and Management Capability Enhancement" seminar was successfully held at the Xi'an International Expo Center. The attendees discussed the important role of laboratory management in the lifecycle management of pharmaceutical companies. By establishing an effective quality control system and promptly identifying potential problems through laboratories, the management level of pharmaceutical companies can be effectively improved. In the future, with the changing market environment and the upgrading of global drug regulatory regulations, the compliance of laboratory management will become increasingly important. How to better meet the development needs of pharmaceutical companies has become a hot topic of discussion in the industry. During the meeting, industry professionals gave presentations and had in-depth discussions on laboratory data management, risk management, clean room testing, validation methods, and other related topics. Suxin Environment participated in the meeting and placed instruments on site for communication.

  
On October 17th, Zhou Yuan, the Product Training Director of Suzhou Suxin Environmental Technology Co., Ltd., presented a report titled "Cleanroom Testing Helps Drug Quality Management" at the "2024 Pharmaceutical Enterprise QC Laboratory Compliance and Management Capability Enhancement" seminar. The report explained the various cleanliness level standards in cleanroom testing, as well as various testing equipment and usage, such as dust particle counters, floating bacteria samplers, air volume meters and other instruments, on how to efficiently and intelligently analyze and detect controlled environments, safeguard the production and manufacturing process, and ensure the cleanliness of cleanrooms.

  
On the morning of October 17th, the Shanghai Indoor Environment Purification Industry Association and APi China jointly held the "2024 API China Drug Production Controlled Environment and GMP Knowledge Competition". The competition aims to improve the technical level of national pharmaceutical and clean enterprise employees in ensuring drug production quality, and better explore, cultivate, and motivate outstanding talents in the industry. Director Zhou Yuan from Su Xin Environment participated in the competition and won fourth place.

  

With the conclusion of the 91st API China, industry professionals will continue to explore the boundaries of technology and promote the integrated development of upstream, midstream, and downstream enterprises in the pharmaceutical industry. SuXin Environment will also respond to the challenges of cleanliness in the new era with a perfect attitude and technology, and provide SuXin's answer. SuXin Environment will use clean technology to assist in drug quality testing and management, and looks forward to the continuous development of clean technology to better safeguard the production and manufacturing process.


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