Harbor
Runharbor provides an AI-powered eClinical data management platform that automates clinical trial workflows from protocol drafting to database lock. The platform's Magic Build engine parses protocol PDFs to instantly generate Case Report Forms and source documents, while Magic Monitor acts as an automated CRA assistant that reviews study data against source records. Pricing starts at $2,000 per month for commercial studies, with a free tier for academic and non-profit research.
- Healthcare Technology
- Artificial Intelligence
- Software Only
Funding
Raised to date
$500KRaised to date based on public sources. This may differ from the amount the company actually raised and is based only on what is publicly available on the internet.
Founders
Founder details are not available yet.
Product
Problem
Clinical trial teams face significant delays and high costs when building electronic data capture (EDC) systems, with database builds often taking weeks or months. Legacy systems require extensive manual data entry and source document creation, while traditional monitoring approaches demand significant on-site CRA time and resources.
Solution
Runharbor delivers an eClinical data management platform that automates the entire clinical study workflow, from protocol drafting to database lock. The platform's Magic Build engine parses protocol PDFs and automatically generates Case Report Forms (CRFs) and source documents, reducing study startup from months to days. Magic Capture automates data extraction from source documents, eliminating manual entry, while Magic Monitor acts as an AI-powered CRA assistant that reviews study data against original source records to identify potential issues. The platform is designed for regulatory compliance, including 21 CFR Part 11, HIPAA, and GCP, with a continuously validated software development lifecycle.
Target Audience
Primary customers are clinical research organizations (CROs), commercial sponsors running clinical trials, and academic or non-profit research institutions conducting investigator-initiated studies.
Features
- Magic Build engine that parses protocol PDFs and automatically generates CRFs and source documents
- Magic Capture for automated data extraction from source documents, reducing manual data entry
- Magic Monitor, an AI-powered CRA assistant that reviews study data against source records with custom monitoring rules
- Built-in compliance with 21 CFR Part 11, HIPAA, and ICH E6 (GCP), including electronic signatures, audit trails, and access controls
- Continuous validation through a CI/CD pipeline with automated testing, risk assessment (FMEA), and version-controlled validation documents
- Zero Trust security model with no standing employee access to client data, hosted on GCP and AWS with private network infrastructure