EDC

This white paper from Castor explores the importance of choosing an EDC with an API before starting a clinical trial.

From pre-market trials to post-market observational studies, hear from industry experts as they review three different case studies and discuss overcoming the challenges faced by medical device manufacturers today.

This white paper from Castor explores the importance of choosing an EDC with an API before starting a clinical trial.

The need for findable, accessible, interoperable, and reusable clinical research data is growing. Learn more in this white paper from Castor

The benefits of integrating EHR data with an EDC range from reducing duplicate documentation and errors to enriching the clinical dataset with real-world data. Why aren’t more people doing it?

Application programming interfaces (API) are an essential feature of any clinical technology platform, saving researchers time and money

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

Join this webinar and learn how to easily change, review and approve eCRF forms in your test environment, without impacting the production study.

Watch this webinar for tips on how to ensure research continuity during COVID-19 by running your trial with a more decentralized approach.

Learn why myTomorrows utilizes Castor to monitor treatment and assess benefit/risk its users, connecting patients with expanded trial access.