Wet granulating equipment for pharmaceutical industry
In pharmaceutical manufacturing, achieving consistent granule size and composition is critical for drug efficacy and quality. Traditional granulation techniques often struggle with inefficiencies and contamination risks, necessitating advanced solutions to enhance productivity and ensure safety.
Achieve consistent granulation and improve safety standards
The wet granulating equipment by Austar combines Process Analytical Technology (PAT), containment technology, and powder handling expertise to optimize the wet granulating and pellet coating processes. This technology ensures precise granule sizes and consistent compositions by leveraging innovative process designs, fluid technologies, and rigorous automatic control systems. For high toxic or active pharmaceutical ingredient (API) productions, the system includes high containment solutions compliant with OEB3 to OEB5 standards, developed in collaboration with European EHS experts. The equipment also integrates advanced batch management, electronic records and signatures, and audit trails to meet stringent data integrity requirements by FDA, EMA, and WHO. Designed in accordance with GAMP5 guidelines, the automatic control system is supported by high-quality, standardized validation documents. The system comes with robust after-sales support, ensuring timely and professional responses. Applications span a wide range of pharmaceutical manufacturing processes, particularly those requiring high precision and contamination control.
Benefits
- Enhanced productivity through advanced PAT integration
- High containment solutions for toxic API production
- Compliance with FDA, EMA, and WHO data integrity requirements
- Customizable and timely delivery with strict quality management
- Robust after-sales service team for professional support