Decentralized Clinical Trials (DCT)

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

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

Castor explores how clinical researchers improve the participant experience by having good user design in their patient-facing technology

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

In this paper, Castor explores the benefits and challenges of Digital Therapeutics (DTx) trials and provides recommendations on best practices for data collection and management.

Castor advisor Craig Lipset, suggests that you consider DCT technology as three separate tiers. Learn more about these tiers and get started with DCT in 2022 with these pro tips.

Medical device regulations in the EU have recently undergone a major overhaul. Learn the key tenets of MDR by device classification in this fact sheet, and what checklist items must be addressed to be fully compliant.

In this whitepaper, we will look at how EDC, eConsent, ePRO, and APIs enable researchers to easily conduct decentralized and hybrid clinical trials.

Download this eBook to gain a comprehensive overview of eConsent, how it satisfies global regulatory requirements and key considerations for ethics board approval.

Download this case study to learn how Castor responded to the disruptive impact of COVID-19 and helped the COVID-RED study implement decentralized clinical trial methods to recruit over 17,825 participants in just 15 weeks.