Access 1,800+ pre-qualified clinical research sites across 35 countries. Build ultra-segmented data requests and receive verified real-world data, without paying CRO markups.
Traditional site selection is broken. Expensive intermediaries, outdated databases, and manual processes waste months before a single patient is enrolled.
Traditional databases list sites that no longer meet your requirements, leading to wasted viability calls and weeks of back-and-forth that go nowhere.
Paper-based onboarding and manual credential verification can stretch site activation from days into months, delaying patient enrollment and burning budget.
CROs consume up to 30% of your study budget in hidden markups and percentage fees, charging you for their overhead, not your actual research needs.
Sites claim recruitment capacity they can't deliver. Without verified patient data, you only discover the truth once contracts are signed and timelines are committed.
Sponsor Prime gives you precision site selection and direct access to federated real-world data, at subscription rates, not CRO percentages.
Advanced search identifying ideal sites based on real, verified data, not promises. Access 360° site dashboards with team composition, certifications, facility capabilities, and patient populations.
Build ultra-segmented Data Asset Access Requests (DAARs), broadcast to the full network, and receive verified real-world data with guaranteed provenance via federated computing.
Stop relying on self-reported site profiles. Our 360° dashboards give you verified, up-to-date intelligence on every site in the network.
Access real-time, verified data for every site: investigator team and credentials, facility infrastructure, therapeutic expertise, patient population by diagnosis code, and historical trial performance, all in one place.
Every investigator and site is verified via BlueCloud technology before joining the network. GCP certifications, medical licenses, and site ratings are tracked in a GDPR Wallet, ensuring compliance before you ever make contact.
Electronic credential management, virtual site visits with recorded assessments, and built-in protocol e-learning eliminate the paper-based bottlenecks that drag site activation into months. Activate in days.
Need hand-held site selection? Our recruiting service handles identification, feasibility assessment, qualification, and full onboarding at a flat rate of $2,501 per site, with a 90-day refund guarantee if no sites qualify.
Our federated RWD marketplace connects you directly with 1,800+ clinical sites. Build a custom DAAR with filters for age, comorbidities, geography, and biomarkers, and receive verified data samples without any identifiable information ever leaving the source.
Filter by any combination of clinical parameters, demographics, geography, and data type to build a DAAR that fits your exact study requirements.
Full electronic health record data from primary & specialist care, harmonized and standardized.
Insurance & payer claims data providing longitudinal treatment and cost records across populations.
Lab results, genomic markers, serology, and imaging biomarkers segmented by therapeutic area.
Continuous real-world monitoring data from wearables, remote patient monitoring devices, and sensors.
PRO instruments, quality-of-life scores, symptom diaries, and patient preference data.
Virtual visit notes, remote diagnosis data, and digital consultation records from telehealth platforms.
De-identified radiology, pathology, and diagnostic imaging with associated clinical context.
Simultaneous access to data across 35+ countries, ideal for global feasibility studies and multi-regional trials.
Our platform automates the most time-consuming parts of site selection and data access, so your team focuses on science, not logistics.
Define your site requirements or build a DAAR with precise filters: therapeutic area, diagnosis codes, age ranges, comorbidities, data types, and geographic coverage.
Your request is instantly broadcast to the full 1,800+ site network. Qualified sites respond directly, with no middlemen and no weeks of cold outreach.
Review verified dashboards, receive data samples, negotiate directly through the platform, and activate onboarding, all in one secure environment.
Federated Computing ensures all analysis happens at the source. No identifiable patient data is ever transferred, stored, or processed outside the originating site's infrastructure.
Full compliance with European and US data protection regulations. Site-by-site consent managed automatically through the platform.
Our infrastructure meets SOC 2 Type II standards for security, availability, processing integrity, and confidentiality.
Information security management certified to international standards. Data flows are audited, encrypted, and access-controlled at every layer.
Analysis runs on the site's infrastructure. Only aggregated, anonymized results are shared; identifiable data never moves, making re-identification mathematically impossible.
A flat subscription replaces the 20–30% of budget CROs charge. The bigger your study, the more you save.
Start your 30-day free trial today. Access 1,800+ pre-qualified sites and the federated real-world data marketplace, with no CRO fees, no markups, and no commitment.
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