Our SMO plans and organizes high-quality, accurate, cost-effective clinical trials, so that you can conduct a trial immediately. Our Clinical Research Coordinators (CRCs) are excellent at comprehending our clients’ overall clinical assessment procedures, and designing, planning, and implementing your studies. They excel at collecting and analyzing data, and at reporting your findings. We believe that it is essential for CRCs to understand where they are in the course of the study, as this is a cornerstone of achieving high-quality.
* English-speaking staff are available. Proofreading services are also available if needed.
As of Sep. 30, 2017
Contracts by area
Contracts by phase
|Area||Total||Clinical trial phase 1||Clinical trial phase 2||Clinical trial phase 3||Post-marketing surveillance||Clinical research||Medical devices|