The Clinical Trials Network (CTNx) provides an extra layer of oversight between the CROs and Sites.The CTNx team is onsite for the SIV and first visits to ensure the site staff is properly trained on the protocol. Sites have access to the CTNx regulatory/compliance teams and CTNx Sr. Investigators 24/7 for questions/ guidance. All Screened Subjects’ must be sent to the CTNx Compliance Officer for review and approval prior to randomization. Sites will be required to record 1 randomly selected Informed Consent for the CTNx team to review. The CTNx team will monitor IP Temperatures and be notified instantly of any excursions. CTNx will match sites with the best fitting trials for their patient population and capabilities. CTNx assists all sites with Start-Up, IRB Submissions/ Communications, Trial Financials and Data Management.
The Clinical Trials Network (CTNx)
8877 Mentor Avenue
Mentor, Ohio 44060