Empowering Confident Decisions in Global Clinical Trials
Almac’s eCOA (electronic Clinical Outcome Assessment) solution delivers flexible, accurate, and participant-focused electronic assessment capture for global clinical trials.
Designed for flexibility and global scalability, Almac eCOA simplifies data collection, enhances compliance, and reduces burden for both participants and sites – empowering sponsors with real-time, reliable data and premium services at every stage of the study.
Built on Almac’s legacy of regulatory excellence and innovation, the platform is multilingual, configurable, and integrates seamlessly with our industry leading IXRS®3 IRT system. Whether used independently or as part of the Almac Trial Coordinator™ ecosystem, it delivers high-quality, real-time data to power confident trial decisions.
Download eCOA Factsheet
Key Benefits of Almac eCOA
Multimodal Support & Global Scale
- Supports validated scales via ePRO, ClinRO, ObsRO, and ePerFO with modality-specific workflows.
- Enables site, participant, and caregiver input through secure mobile, tablet, or web apps- provisioned, BYOD, or hybrid.
- Scale licensing, translations, linguistic validation and rater services supported by preferred partner program.
Participant-Centric Engagement
- Multilingual, intuitive interfaces reduce training and improve compliance.
- Automated alerts, reminders, in-app notifications, and real-time adherence insights keep participants engaged and studies on track.
Unified Integration with eClinical Systems
- Seamless integration with IRT (including Almac Trial Coordinator™ and IXRS®3 IRT), EDC, CTMS, and medical devices.
- Real-time eligibility checks, visit triggers, and randomisation logic.
- Extendable modules for eConsent and clinical supply management.
Scalable, Regulatory-Ready Technology
- Deployed across 100+ trials in 25+ countries and 250+ sites.
- Multi-language deployment with localised user validation.
- Supports hybrid and decentralised trials in oncology, CNS, and rare disease studies.
Compliance for Global Trials
Almac complies with international standards and regulation, ensuring data security and privacy across all operational regions.
Real-World Impact: Decentralised Trial Success
Discover how the PROTEA trial leveraged Almac’s eCOA platform to enable seamless caregiver reporting and remote monitoring for 500 preterm infants, achieving 88% compliance and just 7.8% dropout across 20 study sites. The platform digitally managed over 13,000 assessments and 196 informed consents, reducing site burden and scaling remote data collection with confidence.
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Why choose Almac eCOA?
Flexible Modular Deployment: Use eCOA independently or as part of the Almac Trial Coordinator™ ecosystem; activate only the modules you need.
Participant-First Design: Intuitive, multilingual, and accessible interfaces drive engagement and compliance.
Expert Service & Support: Almac’s dedicated team delivers full-service operational support and deep integration expertise.
Global Reach & Reliability: Trusted by sponsors and CROs worldwide, with proven results in complex, decentralised, and hybrid trials.
Ready to Transform Your Clinical Trials?
Experience the difference with Almac eCOA – streamline data capture, enhance compliance, and empower confident decisions. Contact us to book a demo.
eClinical Solutions for Clinical Trials
Accelerate your clinical trials with our comprehensive eClinical solutions designed for efficiency, compliance, and patient engagement.