Most platforms focus either on supporting patients (e.g., content,tools, communities) or on data collection for research.
Lumiio unifies these two domains—offering meaningful value to patients while capturing structured data that is compliant, analyzable, and fit for regulatory, clinical, and real-world use.
Tools like personalized education, clinician and trial finders, daily health diaries, and community polling empower patients and foster retention.
Deploys validated surveys, PROMs, and disease tracking modules aligned with regulatory-grade methodologies (e.g., longitudinal, standardized, exportable).
This structure ensures that what is engaging for patients also generates high-quality real-world data for research, trials, and post-market surveillance.
Engagement features improve patient onboarding, long-term participation, and real-time insight generation.
Researchers and sponsors benefit from richer, more complete datasets across the patient journey.
Biopharma can accelerate clinical trial readiness, health economics submissions, and market access with continuous, patient-centered data streams.
Disease-agnostic and modular—can be deployed in rare, chronic,and high-burden diseases.
Supports global reach through multilingual UI, customizable consent, and governance models, aligned with GDPR, HIPAA, and local privacy laws.
The platform enables multi-stakeholder collaboration without compromising patient trust, data control, or scientific rigor.
Supports shared governance models and granular data permissioning, empowering patient groups to co-lead data initiatives while enabling partnerships with industry and academia.
Log symptoms, treatments, and milestones with the Health Diary.
Discover specialists with expertise in your disease, clinical trials, and local services tailored to your condition and location.
Access personalized educational resources tailored to your condition and disease journey.
Share your experiences through polls, stories, and community feedback tools.
Launch targeted campaigns, share curated content, and collect feedback.
Understand emerging trends and needs across your population.
Use real-world evidence to support policy change, funding requests, or care access improvements.
Collect longitudinal, patient-reported data in real time.
Understand natural history, care pathways, and patient preferences.
Partner with advocacy groups on shared priorities and long-term goals.
Offer immediate value to your community at no cost.
Add modules and features like analytics dashboards, longitudinal studies, and integrated research tools.
Work with our team to co-design enhanced features and programs for registries, natural history studies, or clinical trial support.