Reshaping Clinical Trials With Patient Access & Data Intelligence
Cerba Research’s Patient Access & Data Intelligence* has developed a comprehensive global clinical offer to complement central lab activities for a wide range of customers, including pharma, biotech, institutions, medical device, and diagnostic companies. Our solution supports all phases of clinical trials, from clustering an eligible pool of patients to recruiting and following them up remotely. With our worldwide network, we can collect routine data that can be enhanced to design unique clinical evidence.
Digital Patient-Centric Solutions
Through our digital patient-centric solutions, we provide end-to-end support to our customers, making clinical trials more efficient, effective, and patient-centered.
Cerba Research can support you with:
- Patient Identification
- Patient Recruitment for observational study and prospective biospecimen collection
- Patient follow-up through hybrid DCT
- Real-World Evidence
Safety, Regulatory, Quality and Commercial Compliance
Our approach complements traditional CRO services, offering a more comprehensive and integrated solution.
Cerba Research is reinforcing support for a better understanding of clinical research with all stakeholders by offering online training for sponsors, investigators, and participants, to enhance the robustness of our clinical trials. Our quality management system in clinical studies is ISO 9001 certified. In addition to applying our quality management system in France, we expand it to countries where we are currently conducting clinical trials, including Africa.
*These solutions are available in France and in French overseas territories and will gradually be extended to the entire network
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Reach out to our experts and discover how our Digital Patient Solutions can help transform your research and advance health.Contact Us