Fivos provides a HIPAA‑compliant, cloud‑based platform that designs, implements, and operates clinical registries for specialty medical societies, integrating EHR data via HL7/FHIR and delivering analytics dashboards, benchmarks, and patient‑reported outcomes. The service also offers device manufacturers curated real‑world evidence, including standardized data extraction, statistical analysis, and regulatory‑grade reporting through secure APIs and de‑identified data exports.
Funding
Funding not disclosed
Founders
Product
Problem
Medical societies often lack the infrastructure and expertise to build and maintain comprehensive clinical registries, making it difficult to generate quality‑improvement metrics and support value‑based care. Device manufacturers require real‑world evidence for performance monitoring and regulatory submissions, but acquiring high‑quality, longitudinal data is time‑consuming and resource‑intensive.
Solution
Fivos delivers a cloud‑based registry platform that designs, implements, and operates clinical data registries on behalf of medical societies, handling data capture, validation, and long‑term follow‑up. For device manufacturers, the company provides curated real‑world data services that include standardized data extraction, statistical analysis, and regulatory‑grade reporting. The platform integrates with electronic health record (EHR) systems using HL7/FHIR standards and stores data in a HIPAA‑compliant environment. Built‑in analytics generate benchmarks, performance dashboards, and patient‑reported outcome summaries to support quality‑improvement initiatives. An API layer enables seamless export of de‑identified datasets for research or submission to regulatory bodies. Consulting support offers methodological guidance and project management to accelerate study timelines and reduce operational overhead.
Target Audience
Primary customers are specialty medical societies that need robust registries for quality improvement and value‑based care, and medical device manufacturers seeking real‑world evidence to inform product performance and regulatory strategies.
Features
- End‑to‑end registry lifecycle management: protocol design, site onboarding, data collection, and ongoing maintenance
- Secure, HIPAA‑compliant cloud storage with role‑based access controls and audit logging
- HL7/FHIR integration adapters for automated data ingestion from EHRs and practice management systems
- Standardized data model supporting procedure codes, clinical outcomes, and patient‑reported outcome measures (PROMs)
- Advanced analytics suite offering risk adjustment, trend analysis, and machine‑learning‑derived performance insights
- Customizable web dashboards and API endpoints for real‑time data access and export
- Regulatory support services including data cleaning, de‑identification, and preparation of submission‑ready evidence packages