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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...
Castor announces appointment of Brad Hightower, leading clinical trials executive, to its advisory board
Castor announces the appointment of Brad Hightower, a leading clinical trials executive, to its advisory board.
2023 Making a Positive Impact
As we kick-off 2023 with a refreshed mindset, we take inventory of what is important and focus on...
Making Every Data Point Count: The Value of Machine-Readable, FAIR (Meta)data in Clinical Research
Martijn Kersloot, PhD, Product Owner at Castor, gives an introduction into the FAIR Data Principles and highlights why...
3 ways to unlock the value of real-world evidence (RWE)
Learn best practices on RWE, Castor's offerings for collecting RWD, and 3 different RWE case studies from Castor...
2023 Guide to Clinical Data Collection under the EU Medical Device Regulation (EU MDR)
Learn key compliance requirements, data collection tips, and important dates for the EU Medical Device Regulation in this...
AKRN optimizes patient assessment collection with Castor ePRO
Castor's ePRO solution enabled AKRN and Company Z to engage with a participant population that, on their own,...
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