R&D Capabilities

R & D STRENGTH

The company operates Class 100, Class 10,000, and higher‑grade cleanrooms, with a total area of 4,000 square meters. A rigorously controlled production environment, comprehensive testing procedures, highly qualified inspection personnel, and robust data analysis ensure that all physical parameters—such as particulate matter content, microbial limits, leakage, tensile strength, and burst pressure—fully comply with regulatory requirements for sterilization packaging of medical devices.

U.S. DuPont Authorized Partnership