For Sponsors
RIO is a unified site network collaborating with dedicated, experienced investigators across diverse specialties and locations. Our approach is designed to provide exceptional quality, reliability, and efficiency, even for the most complex trials. Discover how RIO's innovative model enhances the quality and effectiveness of every clinical trial.
Optimized Start-Up Process
RIO streamlines the study initiation process with a systematic approach that ensures excellence, even for complex trials. Our digitized systems for source, regulatory, and records management allow us to rapidly start, scale, and optimize your study operations. We support a range of trials, including specialized, decentralized, and hybrid models, and integrate advanced technologies as needed.
From study award to site initiation in less than 30 days, our services include integrated tech for payments and data management, and dedicated clinical data specialists. We also offer training for site staff and ensure seamless alignment with your central IRB or laboratory.
Meet Enrollment Goals
RIO is designed to excel in meeting enrollment and retention goals, especially for high-volume and challenging studies. Our cutting-edge technology team continuously enhances recruitment, screening, consenting, and retention processes for Sponsors, CROs and participants.
Each RIO site benefits from dedicated recruitment staff and is strategically located in diverse communities to ensure broad representation in clinical trials. We offer exclusive access to physician and practice databases, immediate enrollment support, and robust community outreach and diversity efforts. Our in-house advertising solutions surpass central campaigns, and our participant adherence programs, along with specialty care sites, provide access to unique populations and advanced procedures.
Rigorous Oversight & Data Management
RIO has developed a cutting-edge quality oversight model that sets the industry standard. Our in-house clinical data, quality assurance, regulatory, and risk management teams work closely with site staff to drive continuous improvement. They ensure that every aspect of our QA/QC processes complies with FDA regulations, ICH GCP guidelines, state laws, industry standards, and RIO’s rigorous SOPs.
We aim for 48-hour data entry and query resolution, conduct routine and random QA reviews, and perform EDC and source cross-checks. Our commitment includes ongoing training for investigators and site staff, supported by CLIA-certified labs, IATA-certified personnel, and GCP-trained experts.
