Clinical Research Site Services and Performance
At CRU Global, our clinical research site services are designed to support the full lifecycle of clinical trials, from site selection and patient recruitment to data collection and regulatory compliance. We understand that the success of any clinical trial hinges on the performance of the research sites, which is why we have developed a robust network of high-performing sites strategically located across the globe.
Our research sites are equipped with state-of-the-art facilities and staffed by experienced clinical teams dedicated to conducting trials with precision and adherence to the highest industry standards. We offer comprehensive site services, including:
The performance of our research sites Is reflected In our strong track record of successful clinical trials. Our commitment to excellence is evidenced by numerous regulatory inspections and audits, all of which have consistently confirmed the high quality of our site operations.
At CRU Global, we are more than just a service provider; we are a trusted partner in bringing innovative treatments to market. Our focus on delivering exceptional site services and performance ensures that our sponsors achieve their clinical trial goals with confidence and efficiency.
Site Selection and Feasibility
We meticulously choose sites from our network based on their therapeutic expertise, access to patient populations, and proven history of successful trial execution. Our feasibility assessments ensure that each site is fully prepared to meet the specific demands of the study and has an adequate pool of eligible patients to support the required clinical trial.
Patient Recruitment and Retention
Our sites excel in patient recruitment, leveraging a combination of advanced technology and community outreach to identify and enrol eligible participants quickly. We also prioritize patient retention, implementing strategies that keep participants engaged throughout the study.
Regulatory Compliance and Quality Assurance
Our sites operate in full compliance with global regulatory standards, including those set by the FDA, EMA, and other key regulatory bodies. We conduct regular internal audits and quality checks to ensure that all aspects of the trial are performed to the highest standards.
Data Collection and Management
Accurate and timely data collection is critical to the success of any clinical trial. Our sites utilize electronic data capture (EDC) systems to streamline data entry, reduce errors, and ensure real-time access to study data.
Study Management and Coordination
Our centralized study management model allows for efficient coordination between sites, sponsors, and CROs. This approach ensures that studies are conducted smoothly, on time, and within budget.Our study management is enhanced by our proprietary Clinical Trial Management System (ERP), which facilitates real-time, online access to key study metrics. This system enables sites, site managers, sponsors, and CRO representatives to view up-to-date, real time (!) information on patient recruitment and visit statuses, payment details, sample tracking, and more.
Clinical Sites
CRU-GLOBAL clinical sites are fully owned by the CRU-GLOBAL’s national affiliate in each country.
Case Studies
We are a global top enroller in many multicentric studies in different therapeutic areas.
