Video28 September 2023 Understand Barriers to eConsent Adoption from Site and Sponsor Perspectives Decentralized technologies are transforming clinical trials by addressing patient recruitment and engagement challenges. Learn more
Webinar27 September 2023 Product Spotlight: Dive deep into Castor’s eConsent Redefine your clinical trials: Join us on October 25th for a live product spotlight on Castor’s eConsent solution. Learn more
Blog26 September 2023 A Digital-First Mindset Shift on eConsent eConsent plays a pivotal role in optimizing modern clinical trials, but the nuance around its adoption for pharmaceutical and medical device companies remains a consideration for implementation teams. Learn more
Webinar19 September 2023 Navigating successful eConsent adoption from sponsor to site Our on demand webinar with Leanne Walsh from Northern Light Lifescience to dive into the process of eConsent adoption from sponsor to site. Learn more
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
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
Blog12 July 2023 Essity uses Castor eConsent to optimize enrollment Essity needed to recruit participants for a decentralized clinical trial. Deploying virtual methods with the help of Castor, the team was able to successfully create a trial ecosystem that was accessible to all participants. Castor allowed Essity to streamline its clinical operations while also making it easier for participants to navigate the journey from start to finish. 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