We can do all the elements involved in the start-up of domestic and global clinical studies from selection of investigators up to study initiation.
Our experience in clinical research allowed us to accumulate the information enough to establish our IRB database where profiles of investigators in different specialties, site-specific IRB processes and requirements for IRB submission are included. Furthermore, with our healthy relationship with IRB staff of individual sites, we can assist our clients to select the investigators swiftly and reach the goal of IRB approval within the planned timeframe.
(Clinical Trial Agreement)
IRB Activities(Initial Submission)
CTA(Clinical Trial Agreement)
[Updated on June 2017]