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We’re live at SCDM 2025 and ready to show you how REDCap Cloud 2.0 is transforming clinical research. With REDCap Cloud 2.0, sponsors and CROs can see how a study is performing clinically in near real-time—compressing the “white space” between data collection and scientific review. Achieve in days what once took months. Key Capabilities: • True Data Unification – Combine case report forms and RWE on one platform for a single, consistent data layer. • Accelerated Insights – Automated checks and anomaly detection deliver analysis-ready datasets faster. • Universal Study Support – Scale from single-site pilots to complex Phase I–IV programs without tool changes. • Seamless Study Modifications – Implement protocol amendments without halting operations or risking compliance. • Open Architecture – Interoperability with external data sources and partner ecosystems to avoid vendor lock-in. 3 Ways to Connect at SCDM 2025: ✅ Session: “Software Co-Development – Goldilocks Gets What She Wants” Join REDCap Cloud COO Dave Sunderhaft and Pfizer’s Ralph Russo to learn how REDCap Cloud is transforming Clinical Data Management at enterprise scale. ✅ Visit Booth #524: Meet our team and explore next-generation technology driving global change. ✅ Pre-Book Your Demo: Visit our website to schedule your 1:1 demo and consultation.

Your EDC shouldn't need to integrate with 5 other study systems. REDCap Cloud brings electronic data capture, ePRO/eCOA, and eConsent into a single validated platform — one login, one audit trail, one source of truth. Designed for lean medical device teams looking to move faster and cheaper without adding risk.

When the auditor walks in, your team shouldn't be scrambling. They should be ready. REDCap Cloud gives med device clinical teams a complete, 21 CFR Part 11-compliant audit trail — every data point, every edit, every signature — traceable and timestamped from first patient in. Built for the teams where "audit-ready" isn't a project. It's a default.

The commercial team is waiting. The investors are watching. The patients need access. REDCap Cloud lets med device clinical teams go from protocol to live study in days — not the months that legacy EDC platforms require. Drag-and-drop study builds, intuitive form design, and rapid validation mean your team spends less time configuring and more time enrolling. Speed shouldn't require shortcuts. It should come from better architecture.

ISO 14155 just changed, and there was no grace period. The fourth edition — ISO 14155:2026 — published March 23, 2026 and replaced the 2020 edition immediately. Not "phasing in." Not "sunset period." Investigations starting today are already measured against it. Learn more about technology compliance in MedTech research.

You don't have a 30-person data management team. You have three people and a deadline. REDCap Cloud is purpose-built for med device and medtech teams that run complex trials without enterprise headcount. Intuitive study builds. Self-service configuration. No dedicated IT required. Fewer resources shouldn't mean more risk. It should mean a better platform.