Evidence That Reflects Reality
Real-world evidence brings clinical relevance to life sciences by showcasing how treatments perform in routine healthcare settings. We help you design and execute RWE studies that strengthen regulatory, commercial, and clinical impact.
Why This Service Matters
While clinical trials offer controlled insights, RWE bridges the gap between efficacy and effectiveness. It’s vital for regulatory submissions, payer negotiations, and value-based care.
Our Key Capabilities
End-to-end clinical trial management you can trust
📋 Study Design & Strategic Planning
- Feasibility analysis and protocol design
- Observational, retrospective, and prospective models
- Epidemiology and burden-of-illness studies
🏢 Data Collection & Integration
- Electronic health records (EHRs)/li>
- Claims, registries, ePROs, and wearables
- Hybrid models combining RCT and real-world data
🧠 Execution & Oversight
- Site and physician network engagement
- Ethics and regulatory approvals
- Real-time monitoring and QC
📦 Analysis & Reporting
- HEOR and outcomes analytics
- Subgroup, cost-effectiveness, and sensitivity analyses
- Publication strategy and support
🩺 Therapeutic Area Expertise
- Oncology
- CNS & Psychiatry
- Infectious Diseases
- Cardiometabolic Disorders
- Rare & Orphan Diseases