Real World Evidence Solutions | Navitas Life Sciences

Empowering smarter decisions with RWE, decentralized trials, and AI driven insights.

Life Sciences companies seeking to build or scale a registry, validate outcomes with regulatory-grade real world evidence, or operationalize real world data (RWD) in clinical trials, need a partner who understands the scientific, regulatory, and logistical demands of RWD/RWE from day one.

At Navitas Life Sciences, we partner with sponsors across the clinical development lifecycle to deliver fit-for-purpose RWD/RWE solutions, from registry planning and execution to longitudinal data harmonization, analytics, and reporting. Whether your objective is a submission built on RWE frameworks, a post-marketing study, or label expansion based on outcomes in everyday clinical practice, we help sponsors generate the evidence that answers the right questions.

What sets us apart is our ability to operationalize complexity:

• Designing and managing multi-country, disease specific registries with integrated genetic and clinical data
• Supporting sponsors with turnkey real world evidence studies backed by medical experts and centralized registry operation and data coordination
• Delivering real world data pharmaceutical analytics using validated platforms and custom ontologies to meet diverse stakeholder needs

Navitas Life Sciences offers integrated real world evidence solutions that empower pharmaceutical and biotech companies and other organizations to make smarter, faster decisions, whether it's supporting regulatory submissions, validating long term safety, or assessing treatment effectiveness across diverse populations.

Our recent article in Applied Clinical Trials, "Effect of AI/ML, Real World Evidence, and Master Protocols on Trial Success", explores how next-generation technologies and trial models are driving global health progress. It highlights how real world evidence frameworks, AI and ML in healthcare and clinical research, and decentralized clinical studies are reshaping clinical development.

Real World Evidence drive Decisions

At Navitas, we bring together RWD/RWE in clinical trials and registries from EHRs, claims, and patient-reported outcomes, converting them into actionable insights. Whether you're looking at real world evidence expectations or building your next submission strategy, our team ensures the data meets both scientific and regulatory rigor.

Our services range from data standardization and harmonization to metadata-driven system interoperability, data visualization and reporting, statistical analysis, and AI/ML-powered data flow optimization.

Insight rich and Patient-Centric: Our Differentiator

Navitas Life Sciences exemplifies the convergence of technology and clinical expertise, leveraging its significant investments in digital transformation for operational excellence in clinical data management. By harnessing AI, ML, and metadata driven solutions, Navitas empowers its clients to achieve data driven decision making in an increasingly complex clinical research environment. As our industry moves toward a more interconnected and data-centric future, Navitas remains a vanguard of innovation, pioneering solutions that accelerate drug development and improve patient outcomes.

Why Navitas Life Sciences?

We don’t just collect data, we deliver real world evidence solutions that meet the needs of regulators, physicians, and patients alike. Our capabilities span:

• Registry landscape analysis and planning
• Integrated registry operational coordinating and data coordination center capability
• Cross-functional teams experienced in both real world data clinical trials and traditional RCTsHarmonization of Multiple Sources for large studies and Integration into Report-Ready Master Datasets
• Leveraging AI/ML-powered BI tools to enhance pattern recognition and accelerate decision-making in clinical research.
• Incorporating AI and ML into RBM and real-time data analysis to help sponsors and research organizations make data-backed decisions with greater speed and accuracy.

Backed by over 35 years of clinical and regulatory excellence, we are one of the few real world evidence companies that offer end-to-end support from protocol design to post-market studies.

Read here: Effect of AI/ML, Real World Evidence and Master Protocols on Trial Success

Partner with Us

If you're looking to turn real world data into powerful, regulatory grade real world evidence, it's time to work with a partner who understands the science, the technology, and the urgency.

Reach out today to explore how Navitas Life Sciences can support your next real world evidence study, registry initiative, or decentralized trial program.

Learn more about our services and solutions by reaching out to us at This email address is being protected from spambots. You need JavaScript enabled to view it.