dashboard – Dror Berel

🚀 Rapid Deployment & Implementation

From Zero to Production in Weeks - Not Months

Deploy fully validated Teal dashboards for Phase I-IV clinical trials with industry-standard modules
Implement out-of-the-box safety tables (AE summaries, lab trends, exposure analysis) compliant with ICH-E3 guidelines
Configure efficacy endpoints modules (time-to-event, binary outcomes, longitudinal analyses) for regulatory submissions
Integrate CDISC-compliant datasets (SDTM, ADaM) with automated validation and quality checks
Adapt Teal framework to non-standard data sources: real-world evidence, patient registries, observational studies
Deliver GxP-validated environments with complete Installation/Operational Qualification documentation

Bring Your Vision to Life - Bespoke Clinical Visualizations

Design custom patient journey timelines showing treatment progression, dose modifications, and clinical events
Build advanced waterfall plots with RECIST criteria, biomarker overlays, and response annotations
Create interactive swimmer plots displaying multi-therapy timelines, adverse events, and disease milestones
Develop proprietary in-house modules tailored to your therapeutic area (oncology, cardiology, rare diseases)
Package reusable module libraries for standardized company-wide reporting frameworks
Implement branded dashboards matching corporate design guidelines and color schemes
Deliver fully documented and validated custom modules ready for regulatory inspection

Click, Explore, Discover - Next-Generation Clinical Intelligence

Build multi-level drill-down systems: summary → cohort → individual patient with seamless navigation
Embed JavaScript-powered visualizations using Plotly, D3.js, Highcharts for publication-quality graphics
Implement clickable adverse event hierarchies: SOC → HLGT → PT with instant patient listings
Create interactive patient profiles with synchronized timelines, lab values, and treatment history
Deploy real-time filtering and brushing across linked visualizations for exploratory analysis
Add custom tooltips and annotations with patient-level details accessible on hover/click
Enable dynamic report generation capturing user interactions and filter states for reproducibility

Accelerate Insights, Reduce Timelines, Ensure Compliance

Speed to insights: Reduce dashboard development time by 60-80% vs. custom Shiny builds
Regulatory-ready: Built-in validation framework meeting FDA/EMA electronic submission requirements
Cost-effective: Leverage open-source pharmaverse ecosystem with enterprise support
Scalable: Modular architecture grows from pilot studies to multi-study portfolios
User empowerment: Enable clinical teams to explore data without programming knowledge
Future-proof: Active community support and continuous updates from pharmaverse contributors

Pharmaceutical companies: Phase I-IV trial monitoring and regulatory submissions
Biotech startups: Rapid dashboard deployment for investor presentations and data reviews
CROs: Standardized reporting platforms across multiple client trials
Academic medical centers: Investigator-initiated trials and real-world evidence studies
Regulatory agencies: Interactive review tools for submission assessment

Full-stack expertise: R/Shiny + JavaScript + validation + CDISC standards
End-to-end delivery: Requirements gathering → development → validation → deployment → training
Proven methodology: Agile development with 2-week sprint cycles and continuous stakeholder feedback
Knowledge transfer: Comprehensive documentation and team training for sustainable maintenance
Ongoing support: Post-deployment optimization, troubleshooting, and feature enhancements

Situation: Needed a full Teal dashboard built rapidly from scratch.

Situation: Existing in-house visualizations and reports needed to move to Teal.

Work: Re-implemented visualizations and reports within Teal with validated components
Impact: Standardized delivery and validation across modules