Marya PLC Control IV Fluid Formulation System with Agitator Formulation Tank Manufacturer
Introduction
Manufactured by Marya, the PLC Control IV Fluid Formulation System with Agitator Formulation Tank is a versatile and highly efficient solution for pharmaceutical production. This system, despite being named for its IV fluid formulation capabilities, showcases remarkable flexibility. It can adeptly handle the preparation of diverse drug dosage forms, including tablets, capsules, injections, and oral liquids, all within the same setup. The PLC control ensures precise operation, while the agitator in the formulation mixing tank guarantees thorough blending. By using this system, pharmaceutical companies can streamline their production processes, slashing both cost and time associated with producing different dosage forms, and eliminating the need for constant equipment changes.
Classification
1.General preparation system: It is used in the production of preparations with complex processes, such as suspensions, emulsions, liposomes, microspheres and other special preparations.
2.Complex preparation system: It is used in the production of preparations with complex processes, such as suspensions, emulsions, liposomes, microspheres and other special preparations.
3.Biological preparation 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.
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.The system can be fully automatic, with modular design, and its follow-up installation and maintenance is convenient.
2.The system follows ASME BPE and GMP design concepts, meets 3D blind corner requirements, and allows for low residue and continuous production.
3.Before manufacturing the equipment in our factory, we will carry out one-to-one three-dimensional design to rationalize the arrangement of pipelines, valves, instruments, etc. in the system to make the operation of the equipment more user-friendly.
4.The automatic control system of CIP and SIP can be turned on by one key, which can automatically detect the end of cleaning and sterilization, with recipe management, electronic signature, electronic records, audit tracking and other computer functions.
5. When the equipment is running, it can realize controllable production of key process parameters of drugs (such as temperature, dissolved oxygen, PH, etc.), and can automatically detect them and give an alarm when there are special conditions outside the set parameters, so as to avoid quality problems of drugs.
6.The material, process and structure of the equipment meet the requirements of EU PED and FDA certifications. We can provide exquisite pharmaceutical 2L to 15000L tanks made of stainless steel, with internal 316L materials. The tank's Ra is less than 0.4μm, with electrolytic polishing process, no hard-to-clean places.
7.We use a sterilizing-grade liquid filter which is made of polyethersulfone (PES), resistant to solutions of pH 1-14 and temperature up to 150ºC, and has good resistance to organic solvents. It has excellent filtration performance and reliable bacteria rejection ability, fully meeting the filtration requirements of pharmaceutical processes.
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 |