Global security and compliance
One platform.
Total control.
A single platform that brings together EDC, Randomization, ePRO and eConsent into a continuous data ecosystem, enabling real-time intelligence across the full lifecycle of IIT/IIS, RCT and RWE studies.
Build and scale your trials with confidence
Simple by design, yet powerful enough for complexity. REDCap Cloud’s EDC gives you a true enterprise-grade platform to design and deploy single-site IIS studies, registries, and everything in between. Manage clinical and RWD data sources while leveraging global libraries and standards to ensure consistency, and governance across the entire trial life-cycle.
Integrate your Data
Capture & Manage all your Clinical Trial data. REDCap Cloud has 100’s of available API’s and eSource to help integrate your data at scale.
Eliminate data silos, dramatically reduce Source Data Verification (SDV) costs, while ensuring clean, compliant regulatory-grade data.
Find the details in your data that matter
REDCap Cloud’s reporting and analytics platform delivers real-time operational and data insights – giving you complete view of site and study performance.
Focus Areas
Start simply. Scale endlessly.
One integrated clinical research platform to unify the clinical research ecosystem, delivering continuous, end-to-end data flow into real-time analytics – powering faster insights, stronger compliance and smarter decision making.
Industry
Sponsors & CROs
Therapeutic Areas
Metabolic & GLP-1
Cardiovascular
Frequently Asked Questions (FAQ)
What is the difference between REDCap Cloud and REDCap [academic]?
REDCap Cloud and the academic REDCap share common lineage but serve fundamentally different markets.
The academic REDCap is a Vanderbilt-licensed software package that each institution installs, hosts, secures, patches, and supports with its own IT staff and infrastructure; with its license explicitly excluding commercially funded projects, data sharing, and third-party access.
REDCap Cloud is a fully validated commercial clinical data platform built for regulated research and delivered as a fully managed Software-as-a-Service (SaaS) that bundles hosting, security, compliance, support, and updates into a single subscription. It unifies EDC, eConsent, eCOA/ePRO, randomization, and medical coding in one platform with the validation documentation, audit trails, and global infrastructure that sponsors, CROs, and regulators require.
Is REDCap Cloud compliant with regulatory frameworks?
Yes. REDCap Cloud is built and validated to meet the regulatory standards that govern global clinical research.
The platform is fully 21 CFR Part 11 compliant for electronic records and signatures, supports ICH GCP E6(R3) and EU Annex 11 requirements for computerized systems, and is HIPAA and GDPR compliant for protected health and personal data.
Every study runs on a validated, version-controlled build with complete audit trails, role-based access controls, and electronic signatures suitable for sponsor audits and regulatory inspection by FDA, EMA, MHRA, and other agencies.
Additional key compliance and security certifications include, but not limited to, HITRUST, ISO 27001, ISO 27017, ISO 27018, and FISMA.
How much does REDCap Cloud cost?
REDCap Cloud is priced per project, with total cost shaped by scope and complexity.
Key parameters such as number of subjects, study duration, and modules selected (EDC, eCOA/ePRO, Randomization, medical coding, and more), and the level of professional services if required for build, validation, and ongoing support.
Sponsors and CROs typically find REDCap Cloud competitive with and often below comparable commercial-grade EDC platforms, particularly for Academic, MedTech and small- to mid-sized programs. Enterprise agreements are also available for organizations running portfolios of studies.
To learn more about REDCap Cloud pricing, request a custom quote by clicking the link below.
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Start your journey with REDCap Cloud today – scale for tomorrows novel therapies.