Video29 April 2024 The impact of an AI-enabled consent process Exploring how early engagement with trial participants through an AI enabled chatbot can enhance both comprehension and satisfaction. Learn more
White papers & guides5 February 2024 eConsent Readiness Guide in 24 Countries eConsent regulations can vary widely across borders. Download this whitepaper to learn the regulatory stances of 24 countries on use of eSignature and eConsent in clinical trials. Learn more
Blog14 November 2023 10 FAQs on eConsent To gain a deeper understanding of eConsent, we have gathered the 10 most frequently asked questions that address the complexities of adoption, integration, and compliance measures Learn more
Webinar Product Spotlight: Dive deep into Castor’s eConsent This product spotlight webinar will help you gain a deeper understanding of Castor’s eConsent capabilities for patients, sponsors and sites. Learn more
Blog11 October 2023 Don’t Overengineer It: Hybrid Designs Overcome Barriers in DTx Clinical Trials At DTxEast 2023, Castor joined a panel discussion to answer big questions when designing DTx clinical trials Learn more
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
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
Webinar 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