Castor
White papers & guides
eConsent Readiness Guide in 24 Countries
Preparing for Post-Market Clinical Follow-Up Under EU MDR
eConsent Readiness Guide in 18 Countries
Download this whitepaper to learn the regulatory stances of 18 countries...
2023 Guide to Clinical Data Collection under the EU Medical Device Regulation (EU MDR)
The role of structured data science in DCT
What patient experience can learn from the 7 Principles of Universal Design
Using APIs to enhance medical device data capture
DTx Clinical Trials and Data Standardization
In this paper, Castor explores the benefits and challenges of Digital Therapeutics (DTx) trials...
Choosing Your Best Route to DTx Commercialization
In this guide, Castor discusses routes to digital therapeutics commercialization...
Navigating the DTx Regulatory Landscape
The regulations around digital therapeutics (DTx) are constantly changing...
Getting Started with DCT in 2022
Overview of EU Medical Device Regulations
Learn the key tenets of MDR...
How Medical Device Trials Can Benefit From Decentralized Methods
In this whitepaper, we will look at how EDC, eConsent, ePRO...
Capturing and Managing Data in DTx Trials
Download this whitepaper to gain a comprehensive overview...
eBook: eConsent
Download this eBook to gain a comprehensive overview...
Case Study: COVID-RED Uses Castor’s Decentralized eClinical Platform
Download this case study to learn how Castor responded...
Castor is a Major Contender in Everest Group PEAK Matrix® of Decentralized Clinical Trial Products Assessment 2021
Download the “Decentralized Clinical Trial Products PEAK Matrix®”....
eConsent Readiness in 12 Countries
eConsent is imperative for continuing research during the COVID-19 pandemic and beyond...