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
Blog9 September 2022 5 steps for patient engagement and better outcomes in decentralized clinical trials For successful decentralized clinical trials, researchers must encourage patient engagement. Learn 5 steps that modern companies are taking for better outcomes. Learn more
Blog8 March 2022 The future of rare disease research Each rare disease research breakthrough offers the promise of a longer, better life for patients who otherwise may… Learn more
Blog28 September 2021 3 Ways eConsent Tackles the Challenges of Modern Clinical Trials Although eConsent struggled to gain momentum and wider acceptance pre-pandemic, it’s now a major part of clinical research. In this article, learn three ways eConsent addresses the requirements for valid informed consent. Learn more
Blog1 September 2021 The evolution of eConsent Since it was first instituted in the 1960s, written consent to participate in research studies has undergone very little change other than tightening regulations and increased participant education of their rights. Learn more
Blog23 August 2021 What Is eConsent in Clinical Trials? eConsent accelerates enrollment, increases retention, and reduces site burden. Find out why it’s the way of the future for clinical trials here. Learn more
Blog5 August 2021 Three Ways Remote eConsent Improves Trial Efficiency eConsent accelerates enrollment, increases retention, and reduces site burden. Learn why it’s the way of the future for clinical trials. Learn more
Blog26 July 2021 Video Conferencing for Remote eConsent: 5 Reasons to Make the Switch Castor is using video conferencing to meet participant needs and lower site burden in clinical trials. Find 5 benefits here. Learn more
Blog16 July 2021 How to Prepare an IRB Submission for a Remote eConsent Study If you are planning on using eConsent in a trial, you’ll need to include it in your IRB submission. Find out what to include here. Learn more
Blog13 July 2021 Understanding the Nuances of Informed Consent in Clinical Trials Informed consent is a critical aspect of clinical trials. But what criteria must be met? And is there more than one type of consent? Find out here. Learn more