Castor’s Global e-Consent Matrix
Electronic consent is now approved or conditionally approved in 27 of 33 countries assessed in Castor's eConsent Country...
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eConsent Readiness Guide in 24 Countries
eConsent regulations can vary widely across borders. Download this whitepaper to learn the regulatory stances of 24 countries...
eConsent Readiness Guide in 18 Countries
What patient experience can learn from the 7 Principles of Universal Design | White paper
Castor explores how clinical researchers improve the participant experience by having good user design in their patient-facing technology
Getting Started with DCT in 2022
Castor advisor Craig Lipset, suggests that you consider DCT technology as three separate tiers. Learn more about these...
eBook: eConsent
Download this eBook to gain a comprehensive overview of eConsent, how it satisfies global regulatory requirements and key...
eConsent Readiness in 12 Countries
eConsent is imperative for continuing research during the COVID-19 pandemic and beyond, but regulations can vary widely across...
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...
eBook: The Decentralized Clinical Trial Playbook
This playbook is a tool for sponsors and CROs who want to leverage DCT technology to support remote...
Using Decentralized Trial Technology to Ensure Study Continuity and Data Quality During COVID-19 and Beyond
Download this white paper to learn why patient-centric, remote research technologies such as eConsent, EDC, and ePRO are...
