Blue CSO, is clinical site organization committed to efficiency and efficacy of clinical trials at the site level, while ensuring patient safety. Blue CSO was formed by a group of Private Investigators, and Clinical Research Professionals from global Clinical Sites and Academic Institutions. These key leaders discovered the gap widening in the partnership between the CRO and research site due to the demands within the industry. These issues left several research sites struggling to remain FDA Complaint, failing to meet GCP standards, falling behind on accurate and timely data requirements, declines in patient recruitment, and most importantly compromising the safety of patients. As a company we are been committed to reversing those trends to maintain industry standards. ✤✤✤ OUR CAPABILITIES ✤✤✤ ✔ Guaranteed Randomizations ✔ Study Brokerage ✔ Contracts and Budgets ✔ Site Invoices| Payments ✔ Human Resources & Development ✔ 24hour Site Support ✔ Quality Assurance ✔ IRB Submissions ✔ Regulatory Document Maintenance ✔ EDC Entry ✔ FDA| Sponsor Approved Source Document (eCRF Creation) ✔ Investigator-Initiated Study Management ✔ Medical Writing ✔ eTMF |ISF Management ✔ Protocol Training ✔ Inventory Management ✔ Monthly On-Site Visits ✔ Vendor Management ✔ Marketing | Community Outreach ✔ Patient Recruitment