Luminova Labs

Clinical Trial Services

Technology-enabled expertise across the clinical trial lifecycle — from protocol insight to study execution.

What we support

From protocol insight to study delivery.

Independent, technology-enabled services for sponsors, CROs and clinical trial technology organisations.

Protocol Intelligence & Risk Assessment

Structured protocol review covering operational complexity, study risks, patient burden, evidence and amendment impact.

COA Strategy & Licensing Support

COA identification and assessment, eCOA suitability, licensing readiness, tracking, dependencies and study planning.

eCOA UAT & Verification Services

Requirements review, UAT strategy, test planning and cases, execution support, defects, retest, traceability and reporting.

Human Factors & Usability

User journeys, critical tasks, usability requirements, risk identification, test design and evidence-based reporting.

DST Logistics & Deployment Planning

Digital study technology and device logistics planning, country/site considerations, deployment tracking and operational readiness.

Physical Device / Layer Assessment

Assessment of physical setup, device-related workflows, usability and operational risks across the participant and site experience.

Protocol Amendment Impact

Assess how protocol changes may affect eCOA, licensing, logistics, timelines, patient burden and operational risk.

Clinical Technology Consulting

Strategy, vendor oversight, implementation, validation/GxP, delivery governance and process improvement across clinical technology.

Discuss your study