22 years of experience


2200+ projects


210+ NDAs from NMPA, FDA and EMA


preferred CRO of 56 Global Clients


500+ employees and 4 centers of excellence in 20 cities in China and US

Request for Information

 As a specialized CRO providing preclinical consultation and clinical services in China, we're uniquely positioned to help you whether you are:

- A Chinese innovator looking to prepare assets for global out-licensing

- A Western company seeking to in-license promising Chinese assets

- An international biotech looking to accelerate development through initial China studies

- A multinational developing global+China integrated clinical strategies

Our team offers the regulatory expertise, clinical operations excellence, and cross-cultural understanding to maximize your chances of success in this dynamic environment.

Contact us now for a free consultation.

Resources Center
China's CGT Market Opportunity: Accelerating Global Cell & Gene Therapy Development

Date:

2025-04-08
Executive SummaryThe global cell and gene therapy (CGT) market is experiencing unprecedented growth, projected to expand...
Accelerating Innovative Cancer Treatment to Approval Executive Summary

Date:

2025-01-14
GCP ClinPlus delivered comprehensive biostatistical services for an innovative oral  targeted therapy inhibiting cancer ...
FDA's Paradigm Shift_ An Opportunity for Accelerated Clinical Trials in China

Date:

2025-04-10
Breaking News (April 10, 2025): The FDA has announced a groundbreaking initiative to phase out animal testing requiremen...