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The all-in-one platform for decentralized and hybrid clinical trial orchestration.

Curebase is a specialized clinical trial platform designed to facilitate decentralized (DCT) and hybrid study models. In the 2026 market landscape, Curebase distinguishes itself through a dual-layered technical architecture: a high-performance SaaS suite for data collection and a virtual site management layer. The platform solves the 'geographic bottleneck' in clinical research by enabling patients to participate from home or local clinics via 21 CFR Part 11-compliant tools. Its technical core integrates ePRO (Electronic Patient-Reported Outcomes), eCOA (Electronic Clinical Outcome Assessment), and multimedia eConsent workflows with a robust telehealth module. Strategically, Curebase operates as both a software provider and a decentralized site, providing the infrastructure needed for real-world evidence (RWE) generation and diverse patient recruitment. By automating the data flow between remote participants and principal investigators, it significantly reduces study timelines and increases the fidelity of longitudinal data in therapeutic areas ranging from rare diseases to digital therapeutics.
Curebase is a specialized clinical trial platform designed to facilitate decentralized (DCT) and hybrid study models.
Explore all tools that specialize in remote monitoring. This domain focus ensures Curebase delivers optimized results for this specific requirement.
Interactive video and quiz modules built into the consent workflow to ensure participant comprehension before digital signature.
HIPAA-compliant, peer-to-peer encrypted video calling directly within the trial app, including screen sharing for clinical instructions.
Customizable branching logic for participant recruitment that automatically qualifies or disqualifies leads based on protocol criteria.
A cross-platform mobile application architecture that allows participants to use their own iOS or Android devices for data entry.
Direct entry of clinical data at the point of care, eliminating the need for manual transcription from paper to EDC.
Automated data ingestion from wearable sensors and EMR systems to complement traditional clinical trial data.
A unified interface for managing multiple decentralized sites, tracking enrollment, and reviewing adverse events in real-time.
Clinical protocol review and digitization mapping.
Configuration of electronic Informed Consent Form (eICF) with multimedia support.
Setup of ePRO/eCOA questionnaires and notification triggers.
Virtual Site or Hybrid Site investigator assignment within the dashboard.
Integration of wearable device APIs (e.g., Apple Health, Garmin) for passive data collection.
User Acceptance Testing (UAT) for participant and investigator portals.
Deployment of the recruitment landing page and screener logic.
Training for clinical research coordinators on remote monitoring tools.
Launch of the production study environment.
Real-time data monitoring and automated export for statistical analysis.
All Set
Ready to go
Verified feedback from other users.
"Highly praised for its user interface and ability to reach diverse patient populations, though some users note a learning curve for traditional investigators."
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