eConsent Readiness in 12 Countries
eConsent is imperative for continuing research during the COVID-19 pandemic and beyond, but regulations can vary widely across borders. Download this whitepaper to learn the regulatory stances of 12 countries on the use of eSignature and eConsent in clinical trials.
Castor Launches Scalable Patient Enrollment and eConsent Platform to Increase Patient Access and Reduce Recruitment Timelines
Castor’s new eConsent platform will improve remote patient recruitment and enrollment as well as access to diverse populations by decentralizing clinical trials.
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.
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.
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.
The True Value of eConsent
The future of informed consent is digital. Learn about the benefits, the process, the regulatory landscape, and the future of eConsent here.
Castor Inks Big Pharma Deal As Decentralized Trials Business Continues to Show Exponential Growth
Hoboken, New Jersey: March 10, 2021: Castor, a leading provider of clinical trial technology, today announced the signing…
A Guide to Capturing and Managing Data in Digital Therapeutics Trials
This playbook is a tool for sponsors and CROs who want to leverage DCT technology to support remote interactions in their clinical studies.
Why Remote Consent Is the New Normal in 2021
COVID-19 changed the conversation around enrollment and recruitment for clinical trials. Learn how eConsent is helping researchers do more despite restrictions.