Clean dispensing system
Keyword:
Clean dispensing system
Category:
Product details
Real-time online monitoring of liquid preparation process parameters, precise proportional temperature control, high metering accuracy, automatic feeding, water injection, stirring, temperature increase and decrease, nitrogen filling, and liquid transfer to filling control functions. It also features multi-variety production formula management, host computer monitoring system, intelligent gateway, intelligent maintenance, and remote quick fault diagnosis function modules. It complies with GAMP5 computer system design, ensuring real-time data recording, electronic signatures, audit trails, access control, and trend charts, forming traceable and authentic electronic data records that meet regulatory requirements.
Modular design and manufacturing with complete FAT testing. The equipment has high integration, compact structure, beautiful appearance, and low space occupancy. The minimal number of interfaces facilitates improved project execution efficiency and overall project controllability.
Matching containers are customized in design and manufacturing based on pharmaceutical companies' drug production process needs, complying with BPE, GMP, GB150, and other relevant guidelines and regulations. They use structures and accessories that meet GMP requirements, such as manholes without short circuits and hygienic NA interfaces. They are seamless, easy to clean, and have an outer surface that is mechanically polished (Ra≤0.8μm) or sandblasted + electrolyzed for a matte texture, facilitating cleaning and maintenance and reducing light pollution. The inner surface is mechanically polished + electrolyzed to a mirror finish (Ra≤0.4μm), preventing sticking and residue, and making it easy to clean.
The system piping is hygienically designed, with no dead-end blind pipes, ensuring easy cleaning and sterilization of the entire system, high cleaning efficiency, and no cold spots during sterilization. Reliable aseptic assurance is provided; pipelines are installed at a reasonable slope, and drainage tests are performed before leaving the factory to ensure no residue and avoid contamination risks. The patented sampling system allows for multiple samplings after a single sterilization, with closed cleaning and sterilization, greatly reducing contamination during sampling, providing a high level of aseptic assurance and operational convenience.
Main Technical Parameters of the Liquid Preparation System |
|||||
Working Volume |
Pressure |
Temperature |
Level/Weight |
Speed |
Other |
10-25000L |
-0.1~0.5±0.1MPa |
-10~150±0.1℃ |
±5‰ |
0~350±1rpm |
Optional |
Application Areas
Aseptic freeze-dried powder injection preparations, terminally sterilized water injection preparations, large-volume injections, fat emulsions, suspensions, and media preparation, buffer preparation, inactivation, and emulsification in the biopharmaceutical industry.
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