eConsent

Stay on top of the latest trend, best practices, and enabling technology in clinical research space through our latest blogs, webinars, white-papers and more about this topic.

The Catch-22 of eConsent: The Missed Opportunity for Improved Clinical Trials

It’s time to move beyond digital PDFs. Discover how real eConsent can transform trials, reduce dropout, and respect...

16 January 2025

Clinical Trials Aren’t Just About Patients (and That’s Okay)

This article explores the debate between patient-centricity and protocol-centricity in clinical trials, featuring insights from Derk Arts (Castor)...

20 December 2024

A New Perspective on Clinical Research: Accessibility and Innovation

Joost Rigter’s inspiring journey highlights the importance of accessibility in clinical research. From AI-driven tools to simplified communication,...

30 September 2024

Waiver of Consent vs Waiver of Written Consent

One is very common, the other is rarely granted. Learn the key differences between waiver of consent &...

14 November 2023

10 FAQs on eConsent

To gain a deeper understanding of eConsent, we have gathered the 10 most frequently asked questions that address...

11 October 2023

Don’t Overengineer It: Hybrid Designs Overcome Barriers in DTx Clinical Trials

At DTxEast 2023, Castor joined a panel discussion to answer big questions when designing DTx clinical trials

26 September 2023

A Digital-First Mindset Shift on eConsent

eConsent plays a pivotal role in optimizing modern clinical trials, but the nuance around its adoption for pharmaceutical...

Preparing Your eConsent Study for IRB Approval

In this blog we cover how eConsent benefits trials and aligns with IRB ethical commitments, how to prepare...

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...

9 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...

The future of rare disease research

Each rare disease research breakthrough offers the promise of a longer, better life for patients who otherwise may...

28 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....

1 September 2021

The evolution of eConsent

Since it was first instituted in the 1960s, written consent to participate in research studies has undergone very...

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...

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...

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...

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...

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...

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