Regulations

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.

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

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

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.

eConsent is imperative for continuing research during the COVID-19 pandemic and beyond, but regulations can vary widely across borders. Download this whitepaper to learn the regulatory stances of 12 countries on the use of eSignature and eConsent in clinical trials.

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

Learn the full impact of PMCF under the EU MDR and how to best prepare your medical device studies.