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The preparation mixing tank system is a type of pharmaceutical equipment used to mix and dispense liquids, through which 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. It is widely used in sterile or non-sterile pharmaceutical field.
The pre-tested modular equipment provides significant savings on installation, faster delivery, and a high level of flexibility and convenience.
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.
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.
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.
It is used for general small molecule chemical preparation, such as aqueous injection, lyophilized powder injection and so on.
It is used in the production of preparations with complex processes, such as suspensions, emulsions, liposomes, microspheres and other special preparations.
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.
The system mixes and dispenses liquid pharmaceutical preparations. It blends active pharmaceutical ingredients (APIs) with solvents like water for injection (WFI), ensuring precise concentrations through controlled stirring, heating, sterilization, and filtration for both sterile and non-sterile applications.
It features a one-button fully automatic CIP (Clean-in-Place) and SIP (Sterilize-in-Place) system that automatically senses completion, accompanied by recipe management, electronic signatures, audit trails, and batch records for full compliance and production automation.
The system monitors critical parameters such as temperature, dissolved oxygen (DO), and pH. If any metric deviates from predetermined parameters, automated alarms trigger immediately to safeguard product quality.
Modular skid manufacturing and pre-testing significantly decrease on-site installation and qualification timelines, minimize field labor costs, ensure faster delivery schedules, and offer maximum integration flexibility.
True-to-scale 3D engineering optimizes the spatial arrangement of piping, valves, and analytical instrumentation, maximizing ergonomics, ease of operation, and accessibility for maintenance.
The equipment accommodates general formulations (aqueous solutions, lyophilized powders), complex formulations (liposomes, suspensions, emulsions, microspheres), and biological formulations (vaccines, antibodies, blood products, recombinant proteins, and buffer solutions).
