Service Capability
JOINN has over 30 years of experience in drug safety evaluation, and has rich experience. By adopting international (FDA, ICH) technical standards, personalized trial design, and standardized quality management (GLP), JOINN can provide evaluation reports that meet regulatory (GLP) requirements to NMPA of China, FDA of the United States, and other countries.
About joinn
One-stop Solutions for Your Drug Innovation From Early-stage R&D to Cllinical Trials
