JOINN Laboratories has established a quality management system that adheres to international standards (CNAS/ILAC-MRA certification) and holds GLP certifications from China’s NMPA, the US FDA, Japan’s PMDA, Korea’s MFDS, and the OECD. We are also accredited by AAALAC, ensuring that all evaluation materials meet global pharmaceutical registration requirements.

Our company provides non-clinical pharmacology and toxicology research and evaluation services to global clients. We specialize in non-clinical safety evaluation, clinical trials, pharmacovigilance, and more. Additionally, we offer services such as experimental animals, disease model animals, and evaluations for veterinary drugs, pesticides, and medical devices.

At JOINN Laboratories, we uphold our mission: Serving Drug Innovation, Focusing on Safety Evaluation and Monitoring Throughout the Drug Lifecycle. With nearly 30 years of experience, comprehensive multidisciplinary expertise, and a commitment to continuous effort, we provide professional services for new drug preclinical trials, clinical trials, and new drug registration. Our ultimate goal is to ensure patient safety and protect human health.