Patient Recruitment
Patient Recruitment
Our internal database includes 16,000+ prescreened volunteers. This gives us a head start in quickly identifying qualified candidates for cardiovascular clinical trials. Through outreach campaigns and inclusive community partnerships, we maintain a nearly 37% participant diversity rate — a strength for trials targeting heart conditions that disproportionately affect underserved populations.
Patient Management
Patient Management
Our approach focuses on building trust and reducing friction for patients at every touchpoint. We offer flexible visit scheduling to accommodate participants' work and family obligations. When transportation is a barrier, we arrange complimentary rides to and from our site. Every patient receives personalized communication and dedicated support throughout their study experience. These patient-centric strategies directly support our 97% retention rate.
Data Collection
Data Collection
The precision of cardiovascular data is critical, especially when tracking endpoints such as systolic blood pressure, ECG outputs, lipid panels, or adverse cardiac events. At RDI, clinical data is entered into our electronic data capture systems on the same day it is collected, giving stakeholders real-time visibility into site activity and data trends. Our staff's experience with decentralized and hybrid models reduces patient burden, expands study access, and improves protocol compliance without sacrificing the integrity or timeliness of the data collected.
Regulatory Compliance
Regulatory Compliance
Cardiovascular trials often involve complex treatment regimens, co-therapies, and safety protocols that require rigorous attention to detail. Our regulatory team maintains complete compliance with ICH-GCP standards and all sponsor-specific requirements, from initial IRB submission through final site close-out. Whether managing risk mitigation strategies for investigational biologics or ensuring dosing accuracy in combination therapy protocols, we maintain a proactive approach to quality and documentation.
