Are you interested in our technology and services?
Our clinical research services team has 20 years of clinical trials experience, working in drug and device trials. We will support you through the steps for protocol development, navigating the IRB approval process, as well as overall engagement and management of a large trial and team.
We can customize how study subjects are monitored and report the information to the study sponsor or CRO. Moreover, we have the unique capability to capture and export all of the full disclosure data in almost every case.
We look forward to hearing from you, complete the form below to contact a representative about any questions you may have or e-mail firstname.lastname@example.org.