• GMP Production System - Liquid Preparation System
  • GMP Production System - Liquid Preparation System
  • GMP Production System - Liquid Preparation System
  • GMP Production System - Liquid Preparation System
  • GMP Production System - Liquid Preparation System
  • GMP Production System - Liquid Preparation System
  • GMP Production System - Liquid Preparation System
  • GMP Production System - Liquid Preparation System

GMP Production System - Liquid Preparation System

Product Introduction

The GMP-grade Liquid Preparation System is a core supporting unit in the full biopharmaceutical production process, providing stable and compliant liquid preparation support specifically for biological culture, separation and purification, and vaccine inactivation/activation processes, spanning the entire biopharmaceutical production chain. Designed with GMP-compliant concepts and material selection, the system adapts to scenarios from laboratory R&D to large-scale production, ensuring the precision, sterility, and traceability of processes, and serving as a key equipment for biopharmaceutical enterprises to achieve standardized and efficient production.

  • GMP Production System - Liquid Preparation System
  • GMP Production System - Liquid Preparation System
  • GMP Production System - Liquid Preparation System
  • GMP Production System - Liquid Preparation System

Description

Core Functions

- Precisely formulated culture media solutions for biological culture processes

- Supports preparation of functional liquids such as buffers and eluents for separation and purification

- Enables accurate preparation of key reagents like inactivators and activators in vaccine production

- Meets the stringent requirements of sterility and no cross-contamination throughout biopharmaceutical processes

Product Features
  1.  Compliant Design: Fully compliant with GMP and relevant biopharmaceutical industry standards, with materials and structures meeting the requirements of sterile production environments
  2.  Process Compatibility: Covers liquid preparation needs across the entire biopharmaceutical process, enabling seamless integration with upstream and downstream units such as bioreactors and purification equipment
  3.  Precision Control: Equipped with a professional control system for precise regulation of parameters such as temperature, pH, and stirring speed during liquid preparation
  4.  Material Assurance: Constructed with high-quality 316L stainless steel, offering corrosion resistance, easy cleanability, and sterilization resistance
  5.  Scalability: Supports modular configuration and customized design to meet personalized requirements of different production capacities and processes

Application Scenarios

- Production processes of biopharmaceuticals (monoclonal antibodies, recombinant proteins, etc.)

- Production processes of vaccines (viral, bacterial, etc.)

- Production processes of cell therapy products

- Large-scale production processes of other biological products

Basic Parameters

 Item

 Description

 Main Material

 316L Stainless Steel

 Volume Range

 Customizable in multiple specifications (50L-10000L available)

 Control Mode

 Intelligent PLC control system, supporting manual/automatic switching

 Aseptic Grade

 Meets GMP aseptic production requirements, with a local Class 100 environment

 Sterilization Method

 In-situ sterilization (SIP), with a sterilization temperature up to 121℃

 Adapted Process

 Biological culture, separation and purification, vaccine inactivation/activation, etc.

 Agitation System

 Mechanical/magnetic agitation optional, with adjustable speed

 Interface Standard

 Compliant with ISO, DIN and other international standards, supporting sterile quick connections

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