JAFRAL | JAFRAL

JAFRAL's facility is designed to accelerate the journey from concept to clinic through integrated development and manufacturing capabilities. The facility combines scientific expertise, advanced infrastructure, and robust quality systems to support a wide range of biologics. Our capabilities span process, analytical and formulation development, microbial fermentation, upstream and downstream process optimization, scale-up manufacturing (1 L to 200 L), QC release testing, GMP batch documentation, fill & finish operations, and product release. We provide both non-GMP and GMP manufacturing services, enabling smooth progression from early research and process development to clinical-grade production. Manufacturing activities are supported by 11 dedicated cleanrooms ranging from Grade D to Grade A, ensuring flexibility, efficiency, and regulatory compliance throughout the product lifecycle. By bringing development, manufacturing, quality control, quality assurance, and regulatory expertise under one roof, JAFRAL helps partners accelerate timelines, reduce development risks, and bring innovative biologics to market with confidence.