According to Pharmacopoeia of the People's Republic of China (2020 edition), we should build a comprehensive drug testing capability, pay attention to the safety of medicinal raw and auxiliary materials, and provide standard testing services for raw materials and auxiliary materials.

The Medical Device Division strives to provide services for biocompatibility, chemical characterization (leachables study) preclinical large animal experimental research, physico-chemical properties testing and microbial test of implantation and outer communication products classified as category II and III. It is complied with global regulations implementation of GLP quality system of OECD, FDA, NMPA and ISO.

Conduct human clinical tests according to the usage and efficacy of products

Use the skin model, cell model, biochemistry and other methods to evaluate the moisturizing and anti-wrinkle efficacies of products

Write the safety assessment report based on customer's product formula information

Toxicological tests such as skin irritation and eye irritation