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Enterprise Layer Intelligence
Categories/Healthcare & Life Sciences/Embleema
Embleema

Embleema

Founded 2017

Collect and unify clinical trial and real-world health data for medical research

Pricing model

Demo

You can use Embleema to gather and organize real-world health data for clinical studies and post-market medical research. The system pulls electronic medical records from thousands of care facilities, participant-reported outcomes, and wearable device metrics into an audit-ready database. You can quickly configure study protocols using modular drag-and-drop components without writing custom code. Researchers can monitor patient progress continuously, verify compliance across data sources, and maintain transparent participant consent throughout long-term studies while reducing traditional trial management expenses and manual data entry errors.

What Embleema does

Configure study protocols using drag-and-drop componentsAuto-populate electronic case report forms from medical recordsSend automated survey prompts to study participantsReview audit trails and data provenance across clinical sitesExport audit-ready clinical datasets for regulatory reviewCollect digital informed consent from enrolled patientsAuto-populates electronic case report forms to reduce manual data entryConnects clinical records from over 60,000 care centersSyncs continuous sensor metrics from more than 550 wearable devicesAssembles study protocols with drag-and-drop no-code modulesTracks source data lineage to maintain an audit-ready databaseCollects electronic patient-reported outcomes directly through dedicated patient applicationsManages participant consent tracking and compliant data sharing permissions

Pricing breakdown

Pricing model: Book a demo

Frequently asked

Epic Systems EMR, Cerner Health Records, Apple HealthKit, Fitbit API, HL7 FHIR Standards, AWS HealthOmics

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Embleema, real-world data, RWD, real-world evidence, RWE, clinical trials, electronic health records, EHR, ePRO, patient registries, wearable data, Phase IV studies, clinical research, audit-ready data, non-interventional studies