granulation

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.

The working area is separated from the transmission area to achieve clean and closed production from powder to granules, effectively preventing dust and cross contamination, and all parts in contact with materials are easy to disassemble and clean.

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

(1)The control system is equipped with five-level password authorization, which is authorized and managed for monitors, operators, process personnel, maintenance personnel and managers respectively; (2)Meeting the EU CE standards.

Production capacity Granulation and drying:130-300kg/batch Bottom spray coating:114-190kg/batch

▲Higher working platform, better for connecting with FBD to discharge ▲Compact structure ▲Tangential impeller ▲WIP system ▲Good reproducibility ▲Can connect with fluid bed dryer to form a fully closed granulating production line ▲Fully meet FDA,CGMP,GMP ▲Control system can optionally complying 21CFR Part11 requirements

1. With mixing impeller and granulating chopper. 2. Wall mounted installation. 3. With vacuum drying. 4. With lifting cylinder. 5. Imported possitive and negative pressure-resistant shaft seals. 6. Automatic retractable rotating cleaning ball is used for cleaning.

Compact structure Tangential impeller Safety interlocking system WIP system Good reproducibility Fully meet FDA, cGMP, GMP

Space saving High pressure resistance Closed transfer Process control and PAT CIP cleaning