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Understand Barriers to eConsent Adoption from Site and Sponsor Perspectives
Decentralized technologies are transforming clinical trials by addressing patient recruitment and engagement challenges.
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...
Navigating successful eConsent adoption from sponsor to site
Our on demand webinar with Leanne Walsh from Northern Light Lifescience to dive into the process of eConsent...
Preparing for Post-Market Clinical Follow-Up Under EU MDR
Download our White Paper: Preparing for Post-Market Clinical Follow-up (PMCF) under EU MDR (European Union Medical Device Regulation)...
Harnessing the power of Patient-centric Technologies
Decentralized technologies are transforming clinical trials by addressing patient recruitment and engagement challenges.
Castor announces Frans van Houten, former CEO of Philips, as the company’s new chairman of its Board Of Directors
His exceptional leadership experience and extensive industry knowledge in the healthcare and technology industries will be invaluable to...
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...
Essity uses Castor eConsent to optimize enrollment
Essity partnered with Castor and Link2Trials to develop a hybrid trial ecosystem that was accessible to all participants.
Castor welcomes Jeanne Hecht to Board of Directors
Castor, an industry leader in modular, patient-centric, clinical trial technology, today announced the appointment of Jeanne Hecht to...
Product Spotlight: Castor ePRO
In this on-demand webinar we dive into the benefits and capabilities of ePRO, and how Castor’s web and...
AI & Air Hockey – What to expect at DIA?
Listen to our CEO & Founder, Derk Arts, as he reflects on lessons learned from the BIO panel...
Unlocking the potential of GPT-generated eConsent for IRB approval
As the adoption of real-world evidence (RWE) in healthcare continues to grow, and with the FDA embracing these...
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...
The role of patient-centric technologies & tokenization in RWE studies
In this on-demand webinar we join forces with UBC & Datavant to dive deep into patient-centric technologies &...
Considerations for the use of RWE in FDA Assessments
As the adoption of real-world evidence (RWE) in healthcare continues to grow, and with the FDA embracing these...
eConsent Readiness Guide in 18 Countries
Improving Your Consent Process with Generative AI
As the adoption of real-world evidence (RWE) in healthcare continues to grow, and with the FDA embracing these...
Real-World Evidence: The Importance of Standardization & Democratization
As the adoption of real-world evidence (RWE) in healthcare continues to grow, and with the FDA embracing these...
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