Marya GMP Standard Liquid Preparation Systems
with Clean-in-place & Sterilize-in-place
Product Description
Marya's next-generation Liquid Preparation System revolutionizes hygienic processing with integrated Clean-in-Place (CIP) and Sterilize-in-Place (SIP) technology. Designed for pharmaceutical, biotech, and food industries, our automated system eliminates cross-contamination risks while reducing downtime between batches. The self-cleaning nozzles, steam sterilization cycles, and touchless operation ensure compliance with cGMP, FDA, and EHEDG standards. Built with 316L stainless steel and smart validation protocols, it delivers aseptic processing with 99.9% efficiency. Marya's CIP/SIP system cuts water/chemical usage by 30% while maintaining peak productivity-making it the smart choice for sterile liquid manufacturing.
Classification:
1)General formulation system: It is used for general small molecule chemical preparation, such as aqueous injection, lyophilized powder injection and so on.
2)Complex formulation system: It is used in the production of preparations with complex processes, such as suspensions, emulsions, liposomes, microspheres and other special preparations.
3)Biological formulation system: It is used for the preparation of various products of biological engineering technology, such as the semi-finished preparation of antibodies, vaccines, blood products, recombinant proteins and so on, and it can also be used for the preparation of culture medium production, purified buffer solution and other auxiliary liquid.
Design parameters:
Volume |
2~15000L |
Material |
304,316L,904L,TA2 |
Stirring type |
Upper mechanical stirring, lower magnetic stirring |
Stirring speed control accuracy |
Speed range 0~450rpm |
Temperature control accuracy |
Temperature range-10~150ºC |
Pressure control accuracy |
Pressure range-0.01Mpa~0.06Mpa
±0.01MPa |
Weighing control accuracy |
3‰ |
Power supply |
380V 50Hz |
Why Choose Our Formulation System?
- Quality and Compliance: Ensures that your products meet the highest quality standards and regulatory requirements.
- Flexibility and Customization: Adapts to various production needs and scales with ease.
- Efficiency and Cost-Effectiveness: Streamlines operations, reduces resource waste, and lowers overall production costs.
- Safety and Reliability: Minimizes human error and maximizes the safety of your production environment.
