Patient Recuirment & Retention
Patient Recuirment & Retentionout
We have a comprehensive database of sites and various specialists that will facilitate rapid identification of potential investigators. Our clinical staff will also train the site staff on protocol related and technical matters. Furthermore, we can monitor for compliance with the study plan, protocol and IRB review, and control of investigational products, as well as report safety data, inform sites about performance and contractual issues, and serve as a point of contact between site, sponsor, regulatory agencies and ethic committees.