Quri provides a HIPAA-compliant AI engine, Aura, that utilizes fine-tuned generative models to analyze patient data and match individuals to clinical trial eligibility criteria. The platform addresses inefficiencies in patient recruitment and quality control, enabling research sites to streamline operations and enhance access to life-changing treatments.
Funding
Funding not disclosed
Founders
Product
Problem
Clinical research sites face challenges in efficiently identifying eligible patients for clinical trials due to the time-consuming and manual nature of screening patient data against complex inclusion and exclusion criteria. This can lead to delays in study enrollment, increased costs, and slower development of new treatments.
Solution
Quri offers Aura, an AI-powered platform designed to streamline patient recruitment and quality control for clinical research sites. By leveraging fine-tuned generative models, Aura analyzes patient data from various sources, such as medical records and intake forms, to automatically match individuals to relevant clinical trial eligibility criteria. The platform provides comprehensive eligibility reports, enabling research staff to quickly identify potential candidates. Quri also offers tools for automated quality control, ensuring data accuracy and compliance throughout the trial process.
Target Audience
Quri's primary customers are clinical research sites seeking to improve the efficiency and accuracy of patient recruitment, enrollment, and quality control processes.
Features
- StudyMatch AI: Analyzes patient information to identify matches for study criteria, generating detailed eligibility reports.
- AI Scout: Performs batch screening of patient databases (EMR, CTMS, CRMs) to identify eligible candidates.
- MRLink: Provides a HIPAA-compliant web page for patients to securely share their medical records with the research site.
- Sentinel: Automates quality control by detecting deviations, adverse events, and prohibited medications in visit documents.
- TrialTrack: Manages the study pipeline, tracks study status, and sets automated reminders.
- ICF Manager: Identifies missing fields and signatures in informed consent forms, maintaining a log for easy organization.
- RedactAI: Automatically redacts PII from medical records in compliance with 45 CFR 164.514.