IND/Clinical/ GMP manufacture
1、Unique process technology，waste ＜ 20mL
2、Highly automated, capable of automatic exhaust and automatic switchingr waste liquids.
3、Multiple modules are available （flow sensor，On-line DLS）
4、Complete biocompatibility research data on contact materials
5、Production capacity: from 100ml to several tens of liters.
6、Provide equipment GMP validation activities and documentation support
7、Equipments complies with cGMP production requirements and t FDA 21CFR Part 11 requirements