EDC

eConsent plays a pivotal role in optimizing modern clinical trials, but the nuance around its adoption for pharmaceutical and medical device companies remains a consideration for implementation teams.

Our on demand webinar with Leanne Walsh from Northern Light Lifescience to dive into the process of eConsent adoption from sponsor to site.

His exceptional leadership experience and extensive industry knowledge in the healthcare and technology industries will be invaluable to Castor

In this blog we cover how eConsent benefits trials and aligns with IRB ethical commitments, how to prepare your IRB submission for approval, and the future impact of large language models on the informed consent process.

Castor, an industry leader in modular, patient-centric, clinical trial technology, today announced the appointment of Jeanne Hecht to its Board of Directors

An avalanche of data from so many real-world sources is available today, with the promise of more data generated daily—so why not use it?

Castor announces the appointment of Brad Hightower, a leading clinical trials executive, to its advisory board.

Martijn Kersloot, PhD, Product Owner at Castor, gives an introduction into the FAIR Data Principles and highlights why collecting machine-readable data is crucial

Learn key compliance requirements, data collection tips, and important dates for the EU Medical Device Regulation in this white paper.

Castor’s ePRO solution enabled AKRN and Company Z to engage with a participant population that, on their own, might struggle with a technology solution that they’ve never used before.