Our CRO is optimized for complex precision oncology trials

Our establishment has one of the largest pool of treatment naive patients in the world.

Ability to create custom gene panels to support clients need to reduce screening costs

Our state-of-the-art facilities and experienced team enable us to deliver high-quality data at scale, helping to bring innovative treatments to market faster.

50 trial site network, includes cancer centers and hospitals sites.

Led by medical, operational, and regulatory experts experienced in hematology and oncology with deep hematology and oncology experience having managed Phase I-IV trials 

Trials network has a captive audience of 160,000 patients annually 

Integrated  central laboratory services, ensuring seamless logistics, review, and testing

Global Regulatory Affairs and Medica writing for strategic leadership and execution

We collaborate with our clients to ensure compliance with the protocol, SOPs, and regulatory guidelines, emphasizing subject safety and data quality/integrity. We deliver a focused and directed risk-based approach to planning and conducting compliance assessments of regulated operations globally by applying the principles of quality risk management (QRM). We oversee the management of quality issues, fostering a culture of continuous process improvement.

Be confident in your data for the entire duration of drug development with responsive and flexible approach to data management and biostatistics. Our Data Management and Biostatistics Team of experts undertake each study with your goal in mind, preparing your data for submission.