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
Tank Material
Stainless Steel 316L
Temperature Resistance
150ºC
Working Volume
2~15000L
Weighing Control Accuracy
3%
Power Supply
380V 50Hz
Sealing and Protection Levels
IP65
Temperature Control Accuracy
Temperature Range-10~150ºC ±0.2ºC
Stirring Speed Control Accuracy
Speed Range 0~450rpm ±3.0%
Pressure Control Accuracy
Pressure Range-0.01MPa~0.06MPa ±0.01MPa
Transport Package
Wooden Box
Specification
350*180*300
Trademark
Marya
Origin
China
Packaging & Delivery
Package Size
350.00cm * 180.00cm * 300.00cm
Package Gross Weight
3500.000kg
Product Description
Marya China Pharmaceutical Aseptic Drug Formulation System with CIP Station System
Introduction
The formulation system is a type of pharmaceutical equipment used to mix and dispense liquids by adding an API to a solvent such as water for injection, and then formulating it into a pharmaceutical agent that meets the desired concentration after stirring, heating, sterilization and filtration.
Classification
Features
1.Modular design, cost-saving and worry-free. The pre-tested modular equipment provides significant savings on installation, faster delivery, and a high level of flexibility and convenience.
2.Fully automatic running system, intelligent and efficient. The one-button automatic control system of CIP and SIP can automatically detect the end of cleaning and sterilization, with recipe management, electronic signature, electronic records, audit tracking and other computer functions, realizing production automation.
3.Controllable production with key process parameters and visualized monitoring of the production process. When the equipment is running, it can realize controllable production of drugs with key process parameters such as temperature, dissolved oxygen, PH, etc., and automatically detect them and give an alarm when there are special circumstances outside of the set parameters, so as to avoid quality problems of drugs.
4.3D simulation design and rational layout. Before manufacturing the equipment in our factory, we will carry out the same size ratio 3D design to rationalize the arrangement of pipelines, valves, instruments, etc. in the system to make the operation of the equipment more user-friendly.
Introduction
The formulation system is a type of pharmaceutical equipment used to mix and dispense liquids by adding an API to a solvent such as water for injection, and then formulating it into a pharmaceutical agent that meets the desired concentration after stirring, heating, sterilization and filtration.
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 all kinds of products applying 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 production of culture medium, purification buffer and other auxiliary liquid preparation.
4.CIP station system: It is used to assist in the on-line cleaning of tanks and pipelines of various preparation and bioreactor systems, and can be controlled separately or integrated with other systems.
Features
1.Modular design, cost-saving and worry-free. The pre-tested modular equipment provides significant savings on installation, faster delivery, and a high level of flexibility and convenience.
2.Fully automatic running system, intelligent and efficient. The one-button automatic control system of CIP and SIP can automatically detect the end of cleaning and sterilization, with recipe management, electronic signature, electronic records, audit tracking and other computer functions, realizing production automation.
3.Controllable production with key process parameters and visualized monitoring of the production process. When the equipment is running, it can realize controllable production of drugs with key process parameters such as temperature, dissolved oxygen, PH, etc., and automatically detect them and give an alarm when there are special circumstances outside of the set parameters, so as to avoid quality problems of drugs.
4.3D simulation design and rational layout. Before manufacturing the equipment in our factory, we will carry out the same size ratio 3D design to rationalize the arrangement of pipelines, valves, instruments, etc. in the system to make the operation of the equipment more user-friendly.
Product Parameters
| Name | Parameters |
| Working volume | 2~15000L |
| Stirring speed control accuracy | Speed range 0~450rpm ±3.0% |
| Temperature control accuracy | Temperature range-10~150ºC ±0.2ºC |
| Pressure control accuracy | Pressure range-0.01Mpa~0.06Mpa ±0.01MPa |
| Weighing control accuracy | 3‰ |
| Power supply | 380V 50Hz (Note: Other voltages require a transformer) |
| Sealing and protection levels | IP65 |
