Castor White Papers

Access white papers related to clinical research regulations and issues including the MDR, IVDR, the FDA approval process, ISO 14155, and decentralized trials.

White papers & guides

5 February 2024

eConsent Readiness Guide in 24 Countries

eConsent regulations can vary widely across borders. Download this whitepaper to learn the regulatory stances of 24 countries...

White papers & guides

6 September 2023

Preparing for Post-Market Clinical Follow-Up Under EU MDR

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

White papers & guides

eConsent Readiness Guide in 18 Countries

White papers & guides

29 November 2022

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 papers & guides

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...

White papers & guides

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

White papers & guides

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

White papers & guides

27 January 2022

DTx Clinical Trials and Data Standardization

In this paper, Castor explores the benefits and challenges of Digital Therapeutics (DTx) trials and provides recommendations on...

White papers & guides

21 January 2022

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...

White papers & guides

18 January 2022

Navigating the DTx Regulatory Landscape

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

White papers & guides

29 November 2021

Getting Started with DCT in 2022

Castor advisor Craig Lipset, suggests that you consider DCT technology as three separate tiers. Learn more about these...

White papers & guides

12 November 2021

Overview of EU Medical Device Regulations

Medical device regulations in the EU have recently undergone a major overhaul. Learn the key tenets of MDR...

White papers & guides

2 November 2021

How Medical Device Trials Can Benefit From Decentralized Methods

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

White papers & guides

19 October 2021

Capturing and Managing Data in DTx Trials

Download this whitepaper to gain a comprehensive overview of DTx, its regulatory landscape, and routes to commercialization.

White papers & guides

29 September 2021

eBook: eConsent

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

White papers & guides

Case Study: COVID-RED Uses Castor’s Decentralized eClinical Platform

Download this case study to learn how Castor responded to the disruptive impact of COVID-19 and helped the...

White papers & guides

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®” assessment by Everest Group to learn why Castor is a...

White papers & guides

eConsent Readiness in 12 Countries

eConsent is imperative for continuing research during the COVID-19 pandemic and beyond, but regulations can vary widely across...

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