Pharmaceuticals and Fine Chemicals
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Keywords:
Pharmaceuticals and Fine Chemicals
- Product Details
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Aisengke focuses on specialized and compliant purification and industrialization services for pharmaceutical intermediates. Targeting the characteristics of thermosensitive, multi impurity, and multi variety switching pharmaceutical materials, it integrates composite purification processes such as distillation, crystallization, extraction, and membrane separation to accurately remove by-products, solvent residues, and heavy metal impurities, effectively improving product purity and yield.
The project adopts a modular modular EPC delivery mode, which is suitable for the entire stage from pilot research and development to mass production. It is equipped with CIP online cleaning and fully automatic traceability control system to avoid the risk of cross contamination during production changes and fully comply with pharmaceutical production compliance standards. We can customize exclusive purification production lines as needed, upgrade existing equipment, and complete process amplification, engineering construction, and production landing in one stop, helping customers reduce costs and increase efficiency, stabilize product quality, and quickly achieve standardized production of pharmaceutical intermediates.
Core advantages of the project
Process customization: Based on the physical and chemical characteristics, flexibly combine multiple separation and purification units, accurately control the impurity removal effect, and adapt to the purification needs of different pharmaceutical intermediates
Balancing compliant production: meeting the requirements of pharmaceutical production for cleanliness, cleaning, and batch traceability, adapting to flexible production of multiple varieties, and reducing the risk of cross contamination during production changes
Reduce amplification risk: Complete the engineering transformation of small-scale trial processes to solve problems such as yield decline and unstable quality caused by laboratory process amplification
Flexible construction mode: supports both traditional on-site construction and modular installation, with pilot testing as the first option and subsequent iterative expansion to optimize investment costs
Full process EPC delivery: one-stop service for process, equipment, self-control, and on-site implementation, reducing multi-party coordination and shortening project implementation cycle
Scope of Application
Innovative pharmaceutical raw material intermediates, chiral pharmaceutical intermediates, advanced pharmaceutical intermediates, drug solvent recovery and refining, pharmaceutical waste liquid resource purification, etc., covering projects of different scales from laboratory pilot testing, small-scale trial production to industrial mass production.
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