Transform Your Research with AI-Powered Solutions
Our suite of intelligent tools streamlines your research workflow, from data collection to analysis, saving you time and ensuring accuracy.
Comprehensive Solutions for Evidence-Based Research
Our integrated suite of tools supports the complete lifecycle of systematic reviews and meta-analyses, ensuring regulatory compliance and scientific rigor at every step.
LRN Research Assistant
Automated systematic review platform designed for regulatory compliance and scientific excellence.
Regulatory Compliance
- • Complete audit trails for every decision and data point
- • Validated methodology aligned with regulatory requirements
Efficiency Gains
- • 85% reduction in screening time with AI-assisted review
- • Automated data extraction with human verification
Quality Assurance
- • Dual screening and conflict resolution workflows
- • Standardized data collection forms with validation
Key Applications
Clinical Evaluation Reports (CERs)
Streamlined literature review process for medical device documentation
Post-Market Surveillance
Continuous monitoring and documentation of safety data
Regulatory Submissions
Comprehensive documentation for FDA and EMA requirements
LRN Analyst
Advanced statistical analysis and evidence synthesis platform for clinical research and meta-analyses.
Statistical Excellence
- • Comprehensive meta-analysis tools with random and fixed effects models
- • Advanced heterogeneity assessment and sensitivity analyses
Evidence Synthesis
- • Integration of clinical trial data with real-world evidence
- • Automated forest plots and publication-ready visualizations
Reporting Standards
- • CONSORT and STROBE guideline compliance
- • Automated report generation for regulatory submissions
Research Applications
Clinical Trial Analysis
Comprehensive statistical analysis for clinical trial data
Evidence Synthesis
Integration of multiple data sources for robust analysis
Safety Monitoring
Continuous analysis of safety signals and adverse events
LRN ETL Pipeline
Enterprise-grade data integration and transformation platform for clinical research data.
Data Security
- • HIPAA and GDPR compliant data handling
- • End-to-end encryption and secure data transfer
Integration Capabilities
- • Seamless integration with existing clinical systems
- • Automated data standardization to CDISC standards
Scalability
- • Enterprise-ready infrastructure with high availability
- • Real-time processing capabilities for large datasets
Enterprise Solutions
Clinical Data Integration
Unified data pipeline for clinical research systems
Regulatory Compliance
Validated systems for regulatory requirements
Data Standardization
Automated conversion to CDISC SDTM/ADaM standards
Validation & Compliance
Regulatory Framework
- • FDA 21 CFR Part 11 Compliant
- • EMA Requirements
- • ISO 14155:2020
- • MDR 2017/745
Quality Management
- • ISO 13485:2016 Certified
- • GxP Validated Systems
- • Regular Third-Party Audits
- • Continuous Validation Process
Ready to Transform Your Research?
Join leading institutions and researchers who have already revolutionized their workflow with our AI-powered solutions.
Proven Research Impact
Our solutions have supported groundbreaking research across multiple therapeutic areas.
Time Reduction
Average reduction in systematic review completion time compared to traditional methods
Publications
Peer-reviewed publications supported by our platform in the last year
Articles Processed
Scientific articles processed through our AI-powered screening system
Therapeutic Area Expertise
Our solutions have been validated across multiple therapeutic areas and research contexts.
Oncology
- • Clinical trial meta-analyses
- • Real-world evidence studies
- • Safety monitoring
Cardiovascular
- • Comparative effectiveness research
- • Device safety studies
- • Post-market surveillance
Rare Diseases
- • Evidence synthesis
- • Natural history studies
- • Registry data analysis
Implementation & Support
Our dedicated team ensures a smooth transition and ongoing success with your research initiatives.
Success Stories
Harvard Medical School Research Team
"The LRN platform has transformed our systematic review process, reducing our review time by 80% while maintaining the highest standards of accuracy."
Dr. Sarah Chen, Principal Investigator
University of Pittsburgh Medical Center
"The regulatory compliance features have been invaluable for our medical device studies, ensuring we meet all documentation requirements."
Dr. Michael Roberts, Research Director