1. Unique process technology, waste <20 ml 2. Highly automated, capable of automatic exhaust and automatic switching waste liquids 3. Multiple modules are available 4. Complete biocompatibility research data on contact materials 5. Production capacity from 100 ml to several tens of liters 6. Provide equipment GMP validation activities and documentation support 7. Complies with cGMP production requirements and FDA 21CFR Part 11 requirements