Our operational services involve a collaborative strategic design process from product inception to regulatory approval, throughout early clinical trial to New Drug Application. The commitment of our project managers is not limited to our sponsors; they are also equally devoted to patients, physicians, investigators, and regulators. When assembling a team for your study, we take into consideration our trial experience and therapeutic expertise to ensure the right match is designed for your trial.
We provide high level of management and clinical development services for clinical trials across all phases, as well as for medical devices, IVDs and vaccines. In the past few years, WuXi Clinical has built solid and long-term partnerships with our customers by delivering projects on time with high level quality. We help customers implement their product development strategies. Our study start-up team’s delivery has been commended by several sponsors for saving at least 2 months, on average, during site start-up.
Our employees offer full-time operational coverage in the U.S. and China and hence are able to offer our customers 24/7 support.
We provide a full range of clinical services, including：
- Project management
- Site selection and activation
- Patient recruitment services
- Clinical monitoring & site management
- Cross-regional strategic regulatory consulting
- Trial Master Files (TMF) management
- Quality Control services
