Integrated granulation and drying system for pharmaceuticals
Pharmaceutical companies face challenges in maintaining consistency and quality during the granulation and drying phases of tablet production. Efficiently controlling these processes is pivotal to ensuring optimal product quality and meeting stringent regulatory standards.
Automate and optimize granulation and drying
The integrated granulation and drying lines by GEA are tailored solutions designed for efficient, high-quality pharmaceutical production. These systems seamlessly combine fluid bed processing, high shear mixing-granulation, and material handling within a unified framework. Featuring advanced PLC-based automation, the lines offer precise control over granulation and drying processes, enhancing product consistency and reducing downtime. The use of Process Analytical Technology (PAT) ensures real-time monitoring, allowing manufacturers to actively manage critical quality attributes. Integrated CIP features enable efficient and validated cleaning processes, minimizing contamination risks and ensuring compliance with FDA/GAMP guidelines. With options for explosion-proof and pressure shock standards, these systems meet rigorous safety and environmental regulations, making them suitable for diverse pharmaceutical applications.
Benefits
- Improves product consistency with advanced automation
- Reduces downtime with efficient CIP systems
- Ensures compliance with stringent regulatory standards
- Real-time monitoring enhances quality control
- Safety features meet explosion-proof and pressure shock standards