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Designed for solid preparation manufacturing in the pharmaceutical industry, this process equipment combines mixing and drying functions, with broad applicability in the medicine, chemical, and food sectors. It offers dual heating options (electric/steam), PID precision process control, and closed online sampling for enhanced efficiency and traceability. The machine supports expandable configurations including explosion-proof systems, 10/12 bar pressure-resistant design, final dedusting systems, dehumidifiers, WIP systems, and PAT modules. Built to fully meet FDA, cGMP, and GMP requirements, its control system can be customized to comply with 21 CFR Part 11, delivering a compliant and reliable solution for high-criticality production environments.

The active valve bodies feature a symmetrical design, eliminating the risk of scraping or debris generation during docking and opening, thereby reducing material contamination.

Inner surface: mirror polished to Ra ≤ 0.2 μm; Outer surface: brushed finish to Ra ≤ 0.4 μm

The FG fluid Bed Granulator is a pharmaceutical-grade equipment integrating mixing and drying functions in a GMP-compliant, dead-space-free design with polished surfaces, operating under negative pressure for containment. It serves pharmaceutical (including TCM), food and chemical applications.

The equipment can be equipped with three water pipe inlets for users to select. The water outlets can be connected to tees or crosses. With convenient and easy operation, it can be used for several machines simultaneously.

Utilizing PID control with Siemens proportional valves, the air temperature is adjustable from ambient to 120°C. With stable steam supply and proper steam traps, temperature stability is maintained within ±2°C of setpoint to prevent fluctuations and enhance production stability.

The automatic production and automatic cleaning formulas of the equipment support variable process control, and the process parameters of each stage can be set independently to meet the needs of customers' customized processes

The equipment adopts PLC full-automatic control. All operations can be automatically completed by setting process parameters according to user requirements. It can print all process parameters, with true and reliable original records, fully complying with GMP requirements for pharmaceutical production.

Adopting modular design, dry and wet granulation can be achieved by replacing the whole grain knife and sieve. A quantitative feeding mechanism can be configured to improve particle size consistency, and a closed silo can be configured to reduce dust leakage