IV Fluid Manufacturing Plant, LIVPRO-10000

Product Details

The LIVPRO-10000 IV Fluid Manufacturing Plant is a high-capacity pharmaceutical processing system designed for the preparation, mixing, homogenization, filtration, and transfer of intravenous (IV) fluid formulations under controlled hygienic and sterile manufacturing conditions.With a nominal processing capacity of 10,000 litres, the LIVPRO-10000 is designed to meet the requirements of large-scale pharmaceutical manufacturing facilities involved in the production of large-volume parenteral (LVP) solutions and other compatible sterile liquid formulations.Engineered for industrial-scale pharmaceutical operations, the LIVPRO-10000 combines robust equipment construction, advanced mixing technology, temperature-control arrangements, hygienic product-transfer systems, and customizable process automation. Its large processing capacity supports efficient batch preparation and provides a suitable platform for pharmaceutical manufacturers seeking to enhance production capabilities and streamline manufacturing operations.The system is designed with particular emphasis on product quality, operational reliability, process consistency, hygienic construction, contamination control, and ease of maintenance.The LIVPRO-10000 IV Fluid Manufacturing Plant is constructed using premium-quality, pharmaceutical-grade stainless steel materials to ensure excellent corrosion resistance, structural strength, durability, and long-term operational reliability in demanding pharmaceutical liquid processing environments.SS 316 stainless steel is utilized for product-contact components, providing excellent resistance to corrosion and supporting hygienic product handling. SS 304 stainless steel is used for suitable non-product-contact components, ensuring mechanical stability and a robust equipment structure.The carefully selected materials, combined with precision fabrication, hygienic welding, appropriate surface finishing, and sanitary construction, help minimize product contamination risks, facilitate effective cleaning and maintenance, and support applicable pharmaceutical manufacturing and GMP requirements.The vessel design can incorporate suitable sanitary connections, smooth internal surfaces, hygienic drainage arrangements, and appropriate inspection provisions according to the project specifications.