CDISC Member Spotlights highlight the individuals and organizations that make our community strong. Through these profiles, we recognize members who are advancing data standards, driving innovation, and contributing their expertise to improve clinical research worldwide. Interested in sharing your own story?
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Intego Clinical
Intego is a biometrics-focused CRO providing biostatistics, statistical programming, and data management services for clinical trials. Intego helps sponsors transform complex clinical data into consistent, high-quality, submission-ready results by adhering to CDISC Standards such as SDTM and ADaM, ensuring data is precise, reliable, and easily interpretable across studies and organizations. This benefits not only Intego's clients but also the broader scientific community, as their work meets high industry benchmarks. Through standardization and strong delivery processes, Intego supports better regulatory confidence and stronger scientific outcomes.
Faro
Faro provides an end-to-end AI-powered platform that transforms clinical trial design, review, and optimization. Faro’s flagship product, Faro Study Designer, enables sponsors to author protocols in a digitally native, USDM-aligned format, connecting biomedical concepts, controlled terminology, and operational insights into a unified data model. By automating design and analysis workflows, Faro helps sponsors reduce study complexity, improve quality, and accelerate startup timelines across the clinical development lifecycle.
DNDi
The Drugs for Neglected Diseases initiative (DNDi) was born on the frontlines of medical action. DNDi is an international, not-for-profit research and development organization. DNDi discovers, develops, and delivers treatments for neglected patients in poor and vulnerable communities around the world. Their treatments are affordable and patient-friendly – and have already saved millions of lives. With offices on five continents, DNDi works to ensure the people most affected by neglected diseases are part of medical research and development, helping to set priorities, strengthen capacity, and deliver new treatments where they are needed most.
CRS Cube
CRScube is an eClinical technology vendor, offering a unified platform that includes EDC, RTSM, ePRO, eConsent, eSource, CTMS, RBQM, eTMF and Safety Reporting. We believe our role is to simplify data capture, clinical trial management and data analysis processes. We developed our platform to make eClinical solutions easier to set up and update, and closer to the clinical trial workflows users need to follow. There are not truly transformative eClinical solutions on the market, as every EDC must perform the same functions. CRScube has fine-tuned their solutions to truly simplify workflows across the clinical trial execution.