EPINTEK's Clinical Trial Department has established clinical CRO technical teams across multiple centers nationwide and formed cooperative relationships with biostatistics departments of several prestigious medical universities in China. We offer comprehensive capabilities throughout the entire clinical trial process, including project initiation, protocol development, site selection, quality control, and report writing, providing solid clinical data support for product registration.

Our team currently consists of more than 20 members with strong medical and related backgrounds. The team members possess high-quality clinical research experience and an average industry experience of nearly ten years. We have established standard operating procedures (SOPs) in compliance with China’s Good Clinical Practice (GCP) requirements.

The team specializes in both pre- and post-market clinical trials, registration, and clinical evaluations. We have participated in numerous clinical trials for innovative medical devices and IVDs, and have accumulated extensive practical experience and in-depth understanding of the needs and challenges of medical device companies.