Marya Pharmaceutical Oncology Drugs Formulation System with Digital Twin Integration

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Marya Pharmaceutical Oncology Drugs Formulation System with Digital Twin Integration

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

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Product Description

Basic Information

Model NO.

MY-FS

Certification

CE, FDA, GMP, ISO

Control System

Fully Automatic

Treatment Process

Filtration, Ultrafiltration

Tank Material

Stainless Steel 316L

Power Supply

380V 50Hz

Protection Levels

IP65

Origin

China

Pharmaceutical Oncology Drugs Formulation System

This specialized pharmaceutical apparatus is designed for liquid mixing and dispensing operations, enabling the preparation of solutions by combining active pharmaceutical ingredients (APIs) with solvents. Through integrated processes including controlled stirring, heating, sterilization, and filtration, the system produces medicinal solutions at precise target concentrations.

System Classification

General Formulation System: For small-molecule chemical prep (aqueous injections, lyophilized powder).
Complex Formulation System: Handles suspensions, emulsions, liposomes, and microspheres.
Biological Formulation System: For antibodies, vaccines, blood products, and recombinant proteins.

Core Advantages

Modular Design - Cost-Saving & Efficient

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

Fully Automated Operation

Featuring 1-click CIP/SIP with auto-detection, recipe management, e-signatures, and audit trails for full compliance.

Real-Time Process Control

Monitoring critical parameters like temperature, DO, and pH with automated alerts for any deviations.

3D Simulation & Ergonomics

Optimized piping and valve placement through 3D modeling for user-friendly operation.

Key Design Features

Premium Material: 316L stainless steel tanks (2L-15,000L) with electrolytic polishing (Ra<0.4µm).
Sterility Assurance: Sterile ventilation filters and CIP spray balls for aseptic operations.
Safety Systems: Integrated burst discs, safety valves, and pressure gauges for protection.
Efficient Mixing: Choice of electromagnetic magnetic stirrer or top mechanical stirrer.
High-Performance Filtration: Sterilization-grade PES filters resistant up to 150°C.

Technical Parameters

Name	Parameters
Working Volume	2 ~ 15,000L
Material	304, 316L, 904L, TA2
Stirring Type	Upper mechanical / Lower magnetic
Stirring Speed Accuracy	0 ~ 450rpm (±3.0%)
Temperature Accuracy	-10 ~ 150ºC (±0.2ºC)
Pressure Accuracy	-0.01Mpa ~ 0.06Mpa (±0.01MPa)
Weighing Control Accuracy	3‰
Power Supply	380V 50Hz

Workshop & Quality Display

Project Cases & Packaging

Frequently Asked Questions

Q1: What materials are used for the formulation tanks?

The system utilizes high-quality 316L stainless steel for tanks, ensuring compliance with FDA and EU PED standards.

Q2: What is the maximum working volume available?

Our formulation systems support a wide range of working volumes from as small as 2L up to 15,000L.

Q3: How does the system ensure sterility during operation?

It integrates automated 1-click CIP (Clean-in-Place) and SIP (Sterilize-in-Place) processes, along with sterile ventilation and exhaust filters.

Q4: Does the system provide automated monitoring of critical parameters?

Yes, the system provides real-time monitoring and control of temperature, dissolved oxygen (DO), and pH levels with automatic deviation alerts.

Q5: What kind of stirring mechanisms are available?

We offer both bottom-mounted electromagnetic magnetic stirrers and top-mounted mechanical stirrers, both featuring variable frequency speed regulation.

Q6: Is the control system compliant with digital twin integration?

Yes, the system supports advanced automation features including recipe management, audit trails, and 3D simulation for digital twin integration.