With over three decades of experience, and headquartered in the U.S, Navitas partners with pharmaceutical, biotech, government and medical device companies to deliver flexible, technology enabled services that ensure quality, compliance and efficiency across the product lifecycle. Navitas was named a Major Contender in the Everest PEAK Matrix CDM Operations Assessment 2025 and it won the Eco Vadis sustainability award for the second year in a row in February 2026.

Our expertise spans clinical operations, real-world evidence (RWE), regulatory, pharmacovigilance and data management solutions. Navitas’ Clinical Development services include protocol design, clinical trial operations, biostatistics, statistical programming, clinical data management (CDM) and real-world data (RWD) strategies. Navitas has operationalized AI/ML models through its proprietary OneClinical Analytics platform, delivering near real-time, data-driven insights across the clinical trial lifecycle to enhance trial efficiency, strengthen patient safety monitoring and enable predictive analytics for informed decision-making. Our Clinical Data Science team is known for delivering CDISC-compliant datasets, high-quality statistical outputs and integrated clinical study reports that meet stringent regulatory standards.

In terms of patient registries, Navitas has worked closely with U.S Government agencies, biotech companies and non-profit foundations to truly understand what drives their clinical research by actively participating in stakeholder meetings, including Steering Committees. Recognizing the critical role of these relationships, we partner with sponsors to ensure that registry data is of the highest quality, supporting evidence-based decision-making. By taking a teaming partnership approach, we apply mission-centered methods to inform our site and data management strategies.

Our deep knowledge of clinical research practice guides our approach, ensuring registry programs remain compliant with industry standards while adapting to evolving sponsor goals. Through our integrated Registry Operations Coordination Center and Data Coordination Center services, we have enhanced site engagement, streamlined communication among stakeholders and scaled registry operations.

Our 112-member strong industry networks, founded in 2001, serve as innovation hubs for peer-to-peer knowledge sharing and problem-solving, helping shape the future of clinical research and regulatory science. By partnering with Navitas, sponsors gain a trusted partner that drives operational excellence, accelerates clinical development, and delivers strategic insights for better patient outcomes.