Video Kicking-off 2024: A year of optimism & opportunity Listen in for Derk’s take on the JPM conference, and what to expect from a first quarter filled with optimism and opportunities at Castor. Learn more
Webinar Product Spotlight: Castor ePRO In this on-demand webinar we dive into the benefits and capabilities of ePRO, and how Castor’s web and mobile ePRO applications empower your hybrid or decentralized trial. 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
Blog21 November 2022 AKRN optimizes patient assessment collection with Castor ePRO Castor’s ePRO solution enabled AKRN and Company Z to engage with a participant population that, on their own, might struggle with a technology solution that they’ve never used before. Learn more
Blog22 September 2022 AKRN handles mid-study changes in medical device clinical trials with Castor EDC AKRN Scientific Consulting, a medical device CRO, used Castor’s flexible EDC solution to handle constant mid-study changes for their client. Learn more
Blog5 July 2022 Electronic Case Report Forms (eCRFs) in Clinical Trials: Shifting to a Modern Research Paradigm Castor is shifting the research paradigm for eCRF in clinical trials, transitioning from old, inefficient processes to a comprehensive CDMS & DCT platform. Learn more
White papers & guides8 March 2022 What patient experience can learn from the 7 Principles of Universal Design | White paper Castor explores how clinical researchers improve the participant experience by having good user design in their patient-facing technology Learn more
White papers & guides29 November 2021 Getting Started with DCT in 2022 Castor advisor Craig Lipset, suggests that you consider DCT technology as three separate tiers. Learn more about these tiers and get started with DCT in 2022 with these pro tips. Learn more
Webinar Introducing Castor Connect Watch this webinar for tips on how to ensure research continuity during COVID-19 by running your trial with a more decentralized approach. Learn more
Blog15 March 2021 PMCF & RWE: Roles of Medical Device Registry Studies & ePROs Registry studies focused on a specific medical device are a valuable tool to capture the safety and outcomes of the device over its lifetime. Read more here. Learn more