Blog24 September 2024 Unlocking FDA’s Vision for PRO Collection in RWE: Timing, Methods, and Insights Discover FDA’s guidance on collecting PROs for Real-World Evidence (RWE), focusing on timing, methods, and improving data quality. Learn more
Blog11 September 2024 Understanding Phase 4 Clinical Trials: A Critical Component of Post-Marketing Insight to Drugs in the Real-World When it comes to Phase 4 clinical trials, Castor’s cutting-edge Real-World Evidence (RWE) platform is your key to unlocking unprecedented insights. Elevate Your Phase 4 Trials with our user-friendly EDC system that adapts to your unique Phase 4 needs. Effortlessly manage multi-region studies with our flexible platform. Reduce costs and accelerate timelines with our innovative AI solutions. Rest easy with our robust security and compliance features. Learn more
Blog9 August 2024 5 Key Takeaways from the FDA’s Real-World Evidence Guidance A deep dive into the evolving regulatory environment, the innovative approaches emerging in RWE, and the critical importance of precise data utilization Learn more
Blog18 July 2024 Navigating the Evolving Regulatory and Data Landscape A deep dive into the evolving regulatory environment, the innovative approaches emerging in RWE, and the critical importance of precise data utilization Learn more
Event23 May 2024 DIA 2024 Meet us at Booth #2327 June 16 – 20, 2024 | San Diego Convention Center Meet the team at booth #2327 at DIA to discuss your RWE needs, get a demo and see our newest human-in-the loop AI capability in action. Learn more
Blog1 May 2024 Revolutionizing Blood Pressure Monitoring: Insights from Aktiia and Castor’s Collaboration How Aktiia brought their continuous BP device to market by integrating vast amounts of blood pressure data with patient-reported outcomes Learn more
Blog22 March 2024 Measuring the true patient experience in Cancer Trials with ePRO Shedding light on the complexities and advancements in measuring PROs, drug tolerability, and quality of life in cancer trials. Learn more
Blog9 May 2023 Unlocking the power of Real-World Evidence in FDA submissions An avalanche of data from so many real-world sources is available today, with the promise of more data generated daily—so why not use it? Learn more