Castor White Papers

eConsent regulations can vary widely across borders. Download this whitepaper to learn the regulatory stances of 24 countries on use of eSignature and eConsent in clinical trials.

Download our White Paper: Preparing for Post-Market Clinical Follow-up (PMCF) under EU MDR (European Union Medical Device Regulation) now.

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.

In this guide, Castor discusses routes to digital therapeutics commercialization and tools to meet the challenges on the path to market

The regulations around digital therapeutics (DTx) are constantly changing. Learn how DTx providers are trying to overcome these challenges