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 Provides Continued Support to the World Health Organization, Powering the World’s Largest Adaptive COVID-19 Trial
Castor announced continued support for the WHO Solidarity trial, the world’s largest adaptive COVID-19 trial.
Introducing Castor Connect
Watch this webinar for tips on how to ensure research continuity during COVID-19 by running your trial with a more decentralized approach.
Making a Real-World Difference for Patients & Clinical Trials
Learn why myTomorrows utilizes Castor to monitor treatment and assess benefit/risk its users, connecting patients with expanded trial access.
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…
Essential 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.