Runharbor
Automates clinical study data collection, eCRF and source document generation, and source-to-EDC data extraction and monitoring
The product is a cloud electronic data capture platform that automates clinical study data collection by generating eCRFs and source documents from protocol PDFs, extracting data from uploaded source documents into eCRFs, and linking each field to its source for monitoring and traceability. It is sold to clinical operations and data management teams at biotech, pharma sponsors, CROs and research sites that run clinical trials. Compared to legacy EDC systems described as digital paper, it is positioned as automation that compresses build times, reduces manual transcription, and enables remote, risk-based monitoring within a validated environment.
Key features
- Protocol-to-EDC Magic Build generation
- Auto-generate eCRFs and visits
- Auto-generate editable source document templates
- AI extraction from uploaded source documents
- Source-linked eCRF fields for traceability
- Risk-based remote monitoring
- Confidence and relevance scoring per data point
- Side-by-side source and EDC review
- Query management and SDV tracking
- ePRO collection with magic login links
- Randomization configuration and assignment
- MedDRA and WHODrug medical coding
- eSignatures and database lock
- Audit trails and role-based access
- Exports and reports for clinical data
- LinkedIn<0.1/day
- Blog
- Partner program
- Healthcare providers
- Operations teams
- Data analytics teams