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2024: Castor Year in Review
As we close the year, the Castor team shares vital milestones the company has achieved to make patient-centric...
Local Labs in the EDC: Streamlining Safety and Efficacy Insights
Local labs are a vital part of clinical trials, offering fast, cost-effective insights into safety and efficacy. But...
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 &...
Castor Launches “Castor for Impact Program” to Advance Health Equity in Clinical Research
Innovative Program Offers Discounted or Free Access to Clinical Trial Technology, Empowering Underserved Research Areas and Early-Stage Biotech...
How MMI Leveraged Castor to Fulfill MDR Requirements for Their Groundbreaking Microsurgery Robot
Castor provided MMI with a compliant, user-friendly platform that was able to enhance enrollment by over 500% and...
DTx company leverages Castor’s Real-World Evidence platform in Registry study
How Castor’s eClinical system helped a DTx company to collect Real World Evidence for their behavioral disorder treatment
Castor collaborates with Microsoft to bring Practical AI to clinical trials.
Today, Castor announces its collaboration with Microsoft to integrate Practical AI in clinical trials, reducing trial burdens for...
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...
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...
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...
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...
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.
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...
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,...
What to look for in an EDC system: a practical guide for clinical trial teams
An electronic data capture (EDC) system is software used to collect, clean, transfer, process, and store data in...