AI TOOL PROFILE
uMed: Clinical Research and Patient Data Platform
- Healthcare
- Data Management
- Pharmaceutical companies
- Clinical Research Organizations (CROs)
- Healthcare researchers
- Biotech firms
- Medical device companies
Pricing
Pricing was not clearly available from the provided evidence. Buyers should confirm current pricing on the vendor website.
At a glance
- Best for
- Pharmaceutical companies, Clinical Research Organizations (CROs), Healthcare researchers, Biotech firms, Medical device companies
- Key use cases
- Participant Identification and Enrollment, Rapid Qualitative Research, Longitudinal Evidence Generation, Post-Market Safety Monitoring
- Official website
- Visit umed official website
How AI is used
uMed is a clinical research platform designed to address evidence gaps in life science research. It connects researchers with a network of consented patients and verified clinical datasets to support data collection.
The platform is intended for pharmaceutical companies, clinical trial teams, and healthcare research institutions. It links electronic health records (EHR) with patient-reported outcomes to track participants over time.
Researchers can use the platform for various stages of drug development, including natural history characterization, trial design, and post-market safety monitoring. The system includes specialized cohorts for cardiometabolic, Parkinson's, and interstitial lung diseases.
Buyers should confirm how the remote recruitment and data collection workflows align with their specific regulatory requirements and if the available disease cohorts match their target patient populations.
Key Features
ACCESS Cohorts
Prospectively recruited, EMR-linked registries designed to follow patients over time for longitudinal evidence.
AI-Driven Patient Matching
Uses AI and automated tools to identify and enroll eligible participants based on clinical data.
SnapACCESS
A tool for rapid qualitative research designed to deliver patient data insights in under four weeks.
SpanACCESS
Supports continuous, AI-driven longitudinal evidence generation across the product lifecycle.
EMR Integration
Links consented patient records with electronic health records to provide clinical history.
Regulatory Compliance
The platform is HIPAA-compliant and holds certifications including ISO27001 and ISO9001.
Use Cases
Participant Identification and Enrollment
Identifying eligible trial patients through EHR-based screening and remote enrollment.
Rapid Qualitative Research
Gathering insights from verified patient cohorts to support commercial decisions or messaging.
Longitudinal Evidence Generation
Tracking disease progression and treatment response over time using linked clinical and patient data.
Post-Market Safety Monitoring
Supporting pharmacovigilance with linked EMR signal detection.
FAQ
What does uMed do?
- uMed provides a platform that connects consented patients with verified clinical datasets, using EMR-linked registries to help researchers generate real-world evidence.
Is uMed compliant with healthcare data regulations?
- Yes, the platform is HIPAA-compliant and is certified to ISO27001, ISO9001, Cyber Essentials Plus, and the NHS Digital Data & Security Toolkit.
What is the difference between SnapACCESS and SpanACCESS?
- SnapACCESS is designed for rapid qualitative research insights in under four weeks, while SpanACCESS is for continuous, longitudinal evidence generation over a longer period.
Source category: Healthcare
Source subcategory: Data Management
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