Marya Solution Preparation System CIP/SIP Integrated Mixing Equipment with Mixing Tank

Customization: Available
Application: Biotechnology Industry, Chemical industry, Clinical Diagnosis, Food & Beverage Factory, Food Safety, Forensic Science, Pharmaceutical Industry
Capacity: 20000 L/hr

Product Description

Basic Info.
Model NO.
MY-FS
Certification
CE, FDA, GMP, ISO
Control System
Fully Automatic
Treatment Process
Filtration, Ultrafiltration
Warranty of core components
1 Year
Power Supply
380V 50Hz
Tank Material
Stainless Steel 316L
Weighing Control Accuracy
3%
Sealing and Protection Levels
IP65
Temperature Control Accuracy
±0.2℃
Stirring Speed Control Accuracy
±3.0%
Origin
China
Product Description

Solution Preparation System CIP/SIP Integrated Mixing Equipment with Mixing Tank

The Solution Preparation Mixing Equipment is a specialized pharmaceutical apparatus designed for liquid mixing and dispensing operations. This equipment enables the preparation of pharmaceutical solutions by combining active pharmaceutical ingredients with solvents such as water for injection. Through integrated processes including controlled stirring, heating, sterilization, and filtration, the system produces medicinal solutions at precise target concentrations. These systems find application across both sterile and non-sterile pharmaceutical manufacturing environments.

Integrated Mixing Equipment
Integrated Mixing Equipment

Classification

  • General Formulation System: For small-molecule chemical prep (e.g., aqueous injections, lyophilized powder injections).
  • Complex Formulation System: Handles advanced processes: suspensions, emulsions, liposomes, microspheres.
  • Biological Formulation System: For biotech products (antibodies/vaccines/blood products/recombinant proteins) & auxiliary liquids (media/buffers).
Core Advantages

1) Modular Design - Cost-Saving & Efficient

Pre-tested modular equipment reduces installation costs, accelerates delivery, and ensures flexibility.

Modular Design

2) Fully Automated Operation - Smart & Compliant

1-click CIP/SIP with auto-detection for cleaning/sterilization completion. Computerized features: Recipe management, e-signature, e-records, and audit trail for full automation.

Automated Operation

3) Process Control & Real-Time Monitoring

Critical parameter control (temp, DO, pH) with auto-alerts for deviations to ensure drug quality.

Real-Time Monitoring

4) 3D Simulation & Ergonomic Layout

Pre-production 3D modeling optimizes piping, valve, and instrument placement for user-friendly operation.

3D Simulation
Design Features
  • Premium Material: 316L stainless steel tanks (2L-12,000L) with electrolytic polishing (Ra<0.4µm), ensuring compliance with EU PED & FDA standards.
  • Sterility Assurance: Sterile ventilation filters and CIP spray balls for aseptic operations.
  • Safety Systems: Integrated safety devices (burst disc/safety valve) for equipment and personnel protection.
  • Efficient Mixing: Magnetic or mechanical stirrer with variable frequency speed regulation.
  • High-Performance Filtration: Sterilization-grade PES filters resistant up to 150°C.
Product Parameters
Name Parameters
Working volume2~15000L
Material304, 316L, 904L, TA2
Stirring typeUpper mechanical, lower magnetic stirring
Stirring speed control0~450rpm ±3.0%
Temperature control-10~150ºC ±0.2ºC
Pressure control-0.01Mpa~0.06Mpa ±0.01MPa
Weighing control3‰
Protection levelIP65
Quality & Facilities
About Us
Why Choose Us
Workshop
Certificate
Product Category
Project Cases
Customers
Exhibition
Team
Packaging & Shipping
Packaging
Shipping
Frequently Asked Questions
What is the primary function of the Solution Preparation System?
It is designed for mixing active pharmaceutical ingredients with solvents, providing controlled stirring, heating, sterilization, and filtration to produce pharmaceutical solutions at precise concentrations.
Does the equipment comply with international standards?
Yes, the system is designed to meet CE, FDA, GMP, and ISO standards, using 316L stainless steel and FDA-compliant seals like EPDM and PTFE.
How is the cleaning and sterilization process handled?
The system features 1-click fully automated CIP (Clean-in-Place) and SIP (Sterilize-in-Place) operations with automatic detection for completion.
What types of formulations can be prepared?
The system can handle general formulations (aqueous injections), complex processes (emulsions, liposomes), and biological products like antibodies and vaccines.
What are the core technical advantages of the modular design?
Modular design reduces installation costs, allows for pre-testing before delivery, accelerates project timelines, and provides high system flexibility.
What is the accuracy level for temperature and weighing?
The system provides high precision with temperature control accuracy of ±0.2℃ and weighing control accuracy within 3‰.

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