Ziplitics

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.

PRISMA Compliant MDR/IVDR Ready

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.

Meta-Analysis Real-World Evidence

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.

21 CFR Part 11 GxP Validated

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

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.

85%

Time Reduction

Average reduction in systematic review completion time compared to traditional methods

100+

Publications

Peer-reviewed publications supported by our platform in the last year

50M+

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.

Validation & Compliance

Regulatory Framework

Our platform is designed to meet the regulatory requirements of the FDA, EMA, and other global health authorities to ensure that your research is compliant and accurate.

  • PRISMA 2020 Compliant
  • MDR/IVDR Compliant

Quality Management

Backed by peer-reviewed, published studies, our highly accurate (>85%) explainable AI solutions will tell you why it made the decisions it made, keeping you compliant with both US and international regulations.

  • Validated Explainable AI
  • Regular Audits