Continuous granulation and compression line for pharmaceuticals

Optimize your pharmaceutical production with a line that seamlessly integrates granulation, drying, and compression, ensuring high-quality, low-dose tablets while maintaining flexibility and control throughout the process.

Integrates Granulation, Drying, and Compression

The ConsiGma® Granulation and Compression (GC) Lines, offered by GEA, revolutionize pharmaceutical manufacturing by integrating continuous wet granulation, fluid bed drying, and tablet compression into a singular system. Ideal for high-value products like low-dose APIs, orphan drugs, and new chemical entities, these lines cater to the precise needs of pharmaceutical manufacturers. Available in three standard sizes, they efficiently handle throughputs from 5 to 120 kg/h, or 20,000 to 180,000 tablets per hour. Conductor 4.0 software enables seamless process control and comprehensive traceability, ensuring compliance with GMP standards. Materials are managed efficiently with loss-in-weight feeders and twin-screw granulators, while optional configurations offer enhanced dosing, blending, and containment solutions. These lines minimize product loss and eliminate work-in-progress, offering agility with compact design and scalable production capabilities. Cleaning and containment features ensure safe handling of highly potent formulations, supported by customizable options and engineering support to meet diverse processing demands.

Benefits

  • Enhances production efficiency by integrating multiple processes into a continuous line.
  • Minimizes API waste with precise dosing and controlled granulation.
  • Reduces risk of contamination with comprehensive cleaning and containment features.
  • Provides flexibility in production scale with adjustable throughput capacities.
  • Ensures compliance with pharmaceutical standards through reliable control and traceability.

General


Applications
Low dose api,Pharmaceutical tablets,Coating materials,Orphan drugs,New chemical entities
End products
Friable tablet cores,Low-dose pharmaceutical tablets,Novel chemical entity formulations,Orphan drug tablets,Hygroscopic tablet cores
Steps before
Formulation premixing,Dosing
Steps after
Tablet coating,Packing,Sterilization
Input ingredients
low dose API,formulation pre-mix,granulation binder,solvent-free binders
Output ingredients
granules,tablet cores,high value products,orphan drugs,new chemical entities
Market info
GEA is known for its expertise in engineering innovative and sustainable equipment and solutions, focusing on sectors such as food, beverages, pharmaceuticals, and energy, with a reputation for quality, efficiency, and advanced technological applications in industrial processing.

Technical Specifications


Capacity
5–120 kg/h or 20,000 to 180,000 tablets/h
Automation
Conductor 4.0 software controlled
Batch size
Flexible batch size
Binder distribution
Controlled granulation binder distribution
Granule particle size distribution
Control of granule particle size distribution
Loss-in-weight feeder
1 for formulation pre-mix
Compression system
GEA compression system

Operating Characteristics


Batch vs. continuous operation
Inline Continuous
CIP/SIP
CIP 121°C / SIP 135°C
Cleaning method
CIP
Automation level
SCADA
Integrated steps
Granulation,Drying,Compression
Control Software
Conductor 4.0

Material Compatibility


Density/particle size
0.5–2.5 g/cm³ / 50–1000 µm

Physical Characteristics


Compact footprint
Small
Machine sizes
3 standard sizes (throughput from 5 to 120 kg/h)
Integration level
Continuous wet granulation,drying,and compression
Configuration
Modular and customizable

Custom Options


Control panel type
Conductor 4.0 software
Integration possibilities
Continuous wet granulation,drying and tablet compression
Cleaning features
CIP / Containment upgrade
Material handling system
Including containment features
Batch size flexibility
Customizable throughput capacities
Module type
TC coater modules
Solvent capability
Solvent capable
Melt granulation set-up
Available