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Enterprise Layer Intelligence
Categories/Healthcare & Life Sciences/Medable, Inc
Medable, Inc

Medable, Inc

Founded 2016

Manage clinical trial studies, patient consent, and outcomes data across global trial sites

Pricing model

Demo

You can use Medable to design, launch, and run clinical research studies with digital tools. It lets you build clinical trials quickly, collect electronic clinical outcome assessments, and gather digital patient consent. Research teams can monitor participant adherence, track regional site activities, and connect wearable sensors or patient mobile devices directly to studies. Automated agents assist in managing clinical workflows, handling study translations, and organizing site data while maintaining strict regulatory compliance and auditable records across every phase of global drug development programs.

What Medable, Inc does

Design electronic consent forms for research participantsConfigure patient outcome assessment questionnairesTrack participant compliance rates across study sitesExport audit logs for regulatory submissionsReview incoming data from remote medical sensorsCoordinate patient enrollment status updates across trial sitesTranslate trial materials for international study locationsBuild clinical study workflows in a visual studio interfaceCollect electronic clinical outcome assessments from participant devicesCapture informed patient consent digitally across global sitesTrack participant study adherence and alert researchers to missed visitsIntegrate wearable health sensors and medical connected devicesTranslate study protocols into multiple languages automaticallyLog every automated action for auditable regulatory compliance

Pricing breakdown

Pricing model: Book a demo

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Medable, clinical trials, eCOA, decentralized clinical trials, eConsent, patient adherence, clinical research, clinical monitoring, drug development, trial design, GxP compliance, patient reported outcomes, DCT, study conduct, clinical data