Categories
Connect with us on LinkedIn
eConsent Readiness in 33 Countries: Your Global Compliance Roadmap
The definitive whitepaper, "eConsent Readiness in 33 Countries," provides an essential regulatory update for clinical operations, confirming that...
From Gaudí to Global Deployment: Castor Builds Smarter Trials in Barcelona
Join Castor at SCOPE Europe | Oct 14–15 | InterContinental Barcelona (Fira Center)
Castor is heading to SCOPE Europe 2025 in Barcelona to showcase how sponsors can streamline global clinical trial...
Castor Bolsters Remote Study Engagement with Streamlined Participant Workflow
OTP login is now standard in Castor’s eConsent platform. No account setup or passwords to create. Participants receive...
Oncobiomix: Slashing Costs and Elevating Data Quality
Discover how Oncobiomix used an integrated platform for eConsent, EDC, and ePRO to save $100K and streamline data...
Do Patients Really Understand Clinical Trials?
Poor comprehension of informed consent disrupts trials. Here’s how to fix it—with data, tech, and actual patient understanding.
eConsent – Patient View
Castor’s eConsent portal supports video integration, real-time signatures, and hybrid consent workflows to enhance engagement and compliance.
eConsent – Site View
Study coordinators aim to enroll participants efficiently, and by partnering with Castor, they leverage direct-to-patient marketing.
Product Suite – Patient View
Complete consent forms, answer surveys, and communicate with her study team without needing to visit a clinic.
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...
Castor eConsent: Streamlined Participant Onboarding for Trials
Download our eConsent factsheet to view an overview of our services.
How Advanced Neuromodulation Researchers Cut Study Build Time by 63% Using Integrated Trial Technology
This detailed case study reveals the practical strategies and technology solutions that enabled researchers to automate participant screening,...
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)...
2024: Castor Year in Review
As we close the year, the Castor team shares vital milestones the company has achieved to make patient-centric...
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,...
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 &...
The impact of an AI-enabled consent process
Exploring how early engagement with trial participants through an AI enabled chatbot can enhance both comprehension and satisfaction.
eConsent Readiness Guide in 24 Countries
eConsent regulations can vary widely across borders. Download this whitepaper to learn the regulatory stances of 24 countries...
10 FAQs on eConsent
To gain a deeper understanding of eConsent, we have gathered the 10 most frequently asked questions that address...