GMP Grade Viral Service

Our GMP-grade viral vector platform is designed to meet global regulatory expectations, including those of the FDA, EMA, NMPA, and WHO. Facilities are equipped with ISO 5–7 (Grade A–C) cleanrooms under BSL-2 compliance, supporting both adherent and suspension-based manufacturing systems. With upstream bioreactor capacities up to 200 L and downstream aseptic fill-finish capabilities, we operate a fully closed and traceable production system with comprehensive documentation, including batch manufacturing records (BMR), certificates of analysis (CoA), and method validation reports.