A singular focus on cancer
With more than 17 years of continuous operations dedicated to cancer and cancer-related supportive care, you can trust us to expertly design and manage your most complex study. Our study experience includes both domestic and international trials.
We offer a full range of integrated and customized clinical trial services.
including project feasibility, study budget and timeline management, study tracking reports, risk assessment and mitigation and vendor management. read more >
including feasibility & site / investigator selection, study start-up, regulatory document collection, IRB submission, TMF set-up and maintenance, clinical monitoring, and site management. read more >
Study Design & Medical Writing
including protocol writing and review / optimization, clinical study report, ISS/ISE, Marketing Approval Applications (MAA) and New Drug Applications (NDA). read more >
Data Management & Biostatistics
including sample size determination, randomization schedules, statistical analysis plan development, DSMB/DMC establishment and management, TLF programming, and data analysis. read more >
Specialty Supportive Care Services
including endpoint selection, protocol optimization, endpoint training, site educational tools, and outcomes management. read more >