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
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
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
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
News1 February 2023 Castor announces appointment of Brad Hightower, leading clinical trials executive, to its advisory board Castor announces the appointment of Brad Hightower, a leading clinical trials executive, to its advisory board. Learn more
Webinar9 December 2022 Making Every Data Point Count: The Value of Machine-Readable, FAIR (Meta)data in Clinical Research Martijn Kersloot, PhD, Product Owner at Castor, gives an introduction into the FAIR Data Principles and highlights why collecting machine-readable data is crucial Learn more
White papers & guides29 November 2022 2023 Guide to Clinical Data Collection under the EU Medical Device Regulation (EU MDR) Learn key compliance requirements, data collection tips, and important dates for the EU Medical Device Regulation in this white paper. 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