eConsent

eConsent regulations can vary widely across borders. Download this whitepaper to learn the regulatory stances of 24 countries on use of eSignature and eConsent in clinical trials.

Castor explores how clinical researchers improve the participant experience by having good user design in their patient-facing technology

Castor advisor Craig Lipset, suggests that you consider DCT technology as three separate tiers. Learn more about these tiers and get started with DCT in 2022 with these pro tips.

Download this eBook to gain a comprehensive overview of eConsent, how it satisfies global regulatory requirements and key considerations for ethics board approval.

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.

This playbook is a tool for sponsors and CROs who want to leverage DCT technology to support remote interactions in their clinical studies.

This playbook is a tool for sponsors and CROs who want to leverage DCT technology to support remote interactions in their clinical studies.

Download this white paper to learn why patient-centric, remote research technologies such as eConsent, EDC, and ePRO are critical during COVID-19 and beyond.