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 white paper.
The role of structured data science in DCT
The need for findable, accessible, interoperable, and reusable clinical research data is growing. Learn more in this white paper from Castor
What patient experience can learn from the 7 Principles of Universal Design | White paper
Castor explores how clinical researchers improve the participant experience by having good user design in their patient-facing technology
Using APIs to enhance medical device data capture
Application programming interfaces (API) are an essential feature of any clinical technology platform, saving researchers time and money
DTx Clinical Trials and Data Standardization
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.
Choosing Your Best Route to DTx Commercialization
In this guide, Castor discusses routes to digital therapeutics commercialization and tools to meet the challenges on the path to market
Navigating the DTx Regulatory Landscape
The regulations around digital therapeutics (DTx) are constantly changing. Learn how DTx providers are trying to overcome these challenges
Getting Started with DCT in 2022
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.