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Belenko Pharmaceutical Technology (Shanghai) Co., Ltd. (hereinafter referred to as Belenko) is a technology group enterprise providing process solutions for the field of life science, focusing on the R&D and manufacturing of key process equipment and consumables for vaccines, antibody drugs, cell therapy, gene therapy and other biological products. Its products cover upstream cell cultureProcess units and process development services such as one-time storage solution preparation and downstream chromatography, ultrafiltration, filtration, etc.Bailingke is committed to continuously providing customers with high-quality innovative products and solutions, and creating an efficient, safe and competitive biopharmaceutical supply chain ecosystem.Since its establishment in April 2021, Belenko has developed rapidly. It has built a production base for disposable storage fluid consumables for biopharmaceuticals, a production base for chromatography fillers and a research and development center, with more than 400 employees.With strong R&D and production strength, the company has launched a series of products, including disposable solution preparation bags, liquid storage bags, sampling bags, freeze-thaw bags, ultrafiltration systems, solution preparation and storage systems, chromatography fillers, software control systems and other biotechnology related products.Belenko's products have now entered many domestic biopharmaceutical enterprises and are used in antibodies, vaccinesLearn more
In the bright June, BLK is full of vitality and will go to many cities overseas and home to participate in industrial and vertical exhibitions.In the season of awn planting, we look forward to working with all our colleagues in the industry to get something from "awn" and "planting".01•🔜ACHEMA 2024 • ⏰ June 10, 2024-1
Bellenko will participate in the 2024 ACHEMA Expo held in Frankfurt, Germany, from June 10 to 14.Since 1920, the Expo has been held every three years. It is the promoter and pioneer of the development of the international fluid process industry.This year's Ahima will welcome more than 130 countries
On May 16, 2024, the "23rd China Biological Products Conference (CBioPC2024)" was co sponsored by the China Vaccine Industry Association, the Biological Products Branch of the Chinese Preventive Medicine Association, the Vaccine Professional Committee of the Chinese Medical Biotechnology Association, and the Biological Products Professional Committee of the Chinese Society of Microbiology
Before listing, the process development of biological products can be divided into three stages, namely pre clinical stage, phase I and phase II clinical stage, phase III clinical stage and commercial production stage.Generally, the scale of the three stages is not the same, so two process transfers are often accompanied by process amplification.Figure 1 Biological Product Process Development Stage
Considering the difference between small molecule drugs and large molecule drugs is helpful to determine the analysis and test method of E&L.The analysis of extractable and extractable substances (E&L) is essential to determine the relevant toxicological risks and ensure the safety of the drug product.The inspection of extractable substances is helpful to identify those that can pollute or affect the quality of drugs
Antibody drug conjugate (ADC) refers to a class of biotechnology drugs that couple small molecule compounds (Payloads) to targeted antibodies or antibody fragments through linkers.along with
Thanks to the high selectivity and volume removal rate of ProteinA affinity filler for antibodies and the robust impurity removal effect.ProteinA affinity filler is the industry standard for antibody drug production due to the limitations of ProteinA binding capacity and the high level of protein A resin
There is such a special kind of packing in the multi mode chromatography packing family of Bellinturk. With its unique packing structure, it plays the dual characteristics of gel filtration and adsorption chromatography and is specially designed for super molecules.Including MaXtar®COLL400, MaXtar ® COLL700
FDA defines process validation as "establishing documentary evidence that a specific process will continue to produce products that meet predetermined specifications and quality attributes".This regulatory requirement reflects the recognition that product quality may be materially affected by the production process.In order to meet this requirement, the process needs to be fully characterized and
Animal vaccines belong to the category of veterinary biological products. Veterinary biological products are an important part of biological products. Because of many shortcomings of traditional vaccines and the development of science and technology, many new vaccines, including recombinant vaccines, have become the focus of research.Scale of animal health industry I. Genetic engineering vaccine
In the classic three-step method of antibody purification, affinity capture+cation exchange+anion exchange, we have introduced the Berindac anion exchange chromatography medium at an early stage. See [purification tips | anion exchange chromatography medium in antibody separation]. Today, we will focus on the introduction of Berindac cation exchange chromatography medium.Berindac cation exchange
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