Expro clinical trial department has a group of experienced and professional technical personnel and perfect quality management and control mechanism, which can ensure that the implementation of clinical trial can meet the requirements of ICH-GCP and China GCP, and obtain high-quality clinical trial data to satisfy customers’ different needs in clinical trial.
Based on the insight into the field of clinical trial, starting from the design of clinical trial protocol, by studying customers’ need thoroughly and giving play to our professional advantages, Expro would design and implement every clinical trial project carefully and professionally to meet the requirements of National Medical Products Administration (NMPA) for registration, and meanwhile, build up a good foundation for the future market promotion.
Expro has established extensive connection with a number of clinical trial centers across the country. Expro not only has successfully provided clinical trial agency service to the products manufactured domestically, but also to the imported products manufactured in Europe, the United States, Japan and Taiwan.
As a professional and dynamic team, Expro clinical trial department always aims to obtain recognition from our customers through our high-quality services.