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Pharmaceutical Industry

Our advantages are concentrated in equipment that has complex technological requirements and conditions within the pharmaceutical industry.

For example, in the pharmaceutical API production process, mixing and blending equipment used in the synthesis, fermentation, crystallization, and drying processes.

Reactor and crystallizers can be used for the synthesis of antibiotics, hormones, vitamins, and other drug intermediates, as well as for the synthesis of enzymes, proteins, peptides, and other bioproducts;

In the pharmaceutical API manufacturing process, the application of fermentation technology is very important. It can not only improve product yield and quality, but also reduce production costs and environmental load.

The JTRZF fermenter at Jhenten can be used for the production of various biologically active substances such as antibiotics, amino acids, vitamins, proteins, etc.

And in the crystallization and drying process , the JTNB Agitated filter dryer is used for the filtration, washing, drying and other operations of pharmaceutical API, intermediates and other materials to achieve product purification and preparation;


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Fermentation Efficiency Enhancement
Fermentation technology is crucial in the production of pharmaceutical APIs, effectively improving product yield and quality while reducing costs and environmental load.
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Versatile Application
The Jhenten JTRZF fermenter is suitable for the production of various biologically active substances such as antibiotics, amino acids, vitamins, proteins, and more.
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Three-in-One Efficient Processing
The JTNB Agitated filter dryer integrates three functions, achieving purification and drying of pharmaceutical APIs and intermediates.

In terms of handling pharmaceutical liquids and solvent recovery, the Supervapor low-temperature heat pump evaporation system has innovative and energy-saving advantages, and can achieve material evaporation and concentration at lower temperatures, thus protecting the effective ingredients of the drug and improving drug purity. For example, in the production of antibiotics, low-temperature evaporators can effectively remove water or other volatile components from the liquid to help improve the purity and stability of antibiotics, reduce production costs and reduce environmental pollution;

The Supervapor low-temperature heat pump evaporation system is used for the recovery of solvents from raw materials. It uses a small amount of external energy and through heat pump cycle, separates solvents from waste liquid. The advantage of this system is that its operation process does not require external heating medium, but only consumes a small amount of electricity. Therefore, it is particularly suitable for recycling and reuse of solvents in waste liquid.

1
Energy-efficient Evaporation System
Supervapor uses the low-temperature heat pump principle, ensuring an energy-efficient evaporation process that reduces energy consumption.
2
Low-Temperature Concentration to Protect Drug Efficacy
It can achieve evaporation and concentration at lower temperatures, effectively protecting the active ingredients of the drug and improving purity and stability.
3
Antibiotic Purification Tool
Widely used in antibiotic production, it removes moisture and volatiles, enhancing product purity and reducing pollution.
4
No Need for External Heating Medium
The system operates through heat cycling without the need for boilers or steam, consuming only a small amount of electricity.
5
Efficient Solvent Recovery
In pharmaceutical API preparation, it can recover useful solvents from waste liquids, enabling resource reuse and cost savings.
6
Dual Benefits of Cost Reduction and Emissions Reduction
It reduces both production costs and environmental impact, contributing to the green transformation of pharmaceutical processes.

In the pharmaceutical API industry, CIP systems are mainly used for equipment cleaning and disinfection. They can use fixed on-line cleaning equipment for automatic cleaning and disinfection, effectively reducing manual intervention and operating time. At the same time, the application of CIP systems can also improve equipment cleanliness and hygiene standards to ensure the quality and safety of drug production.

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Automatic On-line Cleaning
CIP systems use fixed equipment for automated cleaning and disinfection without the need for disassembly.
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Reduce Manual Intervention
The cleaning process requires no manual operation, improving efficiency and reducing operation time.
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Improve Cleanliness Standards
The system achieves high cleanliness standards, ensuring equipment hygiene and compliance with GMP requirements.
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Ensure Drug Safety
By improving cleanliness, it ensures the quality and safety of drug production from the source.

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