Video24 August 2023 Harnessing the power of Patient-centric Technologies Decentralized technologies are transforming clinical trials by addressing patient recruitment and engagement challenges. Learn more
News21 August 2023 Castor announces Frans van Houten, former CEO of Philips, as the company’s new chairman of its Board Of Directors His exceptional leadership experience and extensive industry knowledge in the healthcare and technology industries will be invaluable to Castor Learn more
Blog14 August 2023 Preparing Your eConsent Study for IRB Approval In this blog we cover how eConsent benefits trials and aligns with IRB ethical commitments, how to prepare your IRB submission for approval, and the future impact of large language models on the informed consent process. Learn more
Success Stories12 July 2023 Essity uses Castor eConsent to optimize enrollment Essity partnered with Castor and Link2Trials to develop a hybrid trial ecosystem that was accessible to all participants. Learn more
News3 July 2023 Castor welcomes Jeanne Hecht to Board of Directors Castor, an industry leader in modular, patient-centric, clinical trial technology, today announced the appointment of Jeanne Hecht to its Board of Directors 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
Video19 June 2023 AI & Air Hockey – What to expect at DIA? Listen to our CEO & Founder, Derk Arts, as he reflects on lessons learned from the BIO panel discussion and what to expect at DIA. Learn more
Video12 May 2023 Unlocking the potential of GPT-generated eConsent for IRB approval As the adoption of real-world evidence (RWE) in healthcare continues to grow, and with the FDA embracing these trials more and more, researchers have come to appreciate the significance of establishing uniform approaches for evaluating and analyzing real-world data (RWD). 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
Webinar The role of patient-centric technologies & tokenization in RWE studies In this on-demand webinar we join forces with UBC & Datavant to dive deep into patient-centric technologies & tokenization in RWE studies. Learn more