Blog

Gain insights and opinions from the latest experts on medical research, clinical practices, and regulatory changes in the tech industry.

Evaluating “Bother” as a Component of Patient-Reported Outcomes in Clinical Studies

Patient-reported outcome (PRO) instruments refer to multiple scales and questionnaires designed to collect patients’ personal feedback on their...

Revolutionizing Blood Pressure Monitoring: Insights from Aktiia and Castor’s Collaboration

How Aktiia brought their continuous BP device to market by integrating vast amounts of blood pressure data with...

5 Best Practices for Getting Started with ePRO

Electronic Patient Reported Outcomes (ePRO) can become a powerhouse for gathering high-quality data directly from patients. To help...

Can BYOD help us end an era of waste and burden in eCOA?

Bring Your Own Device (BYOD) represents the future of eCOA, and prioritizes flexibility & convenience for trial participants....

Measuring the true patient experience in Cancer Trials with ePRO

Shedding light on the complexities and advancements in measuring PROs, drug tolerability, and quality of life in cancer...

The Place of PROs in the Future of Healthcare

Learn how integrating Patient-Reported Outcomes (PROs) into clinical trials can drive success in Value-Based Care (VBC).

20 February 2024

Accelerating AI Innovation in Pharma: Collaboration versus Competition

Should clinical trial companies collaborate to speed up innovation in AI, or is a healthy dose of competition...

14 November 2023

10 FAQs on eConsent

To gain a deeper understanding of eConsent, we have gathered the 10 most frequently asked questions that address...

11 October 2023

Don’t Overengineer It: Hybrid Designs Overcome Barriers in DTx Clinical Trials

At DTxEast 2023, Castor joined a panel discussion to answer big questions when designing DTx clinical trials

26 September 2023

A Digital-First Mindset Shift on eConsent

eConsent plays a pivotal role in optimizing modern clinical trials, but the nuance around its adoption for pharmaceutical...

Preparing Your eConsent Study for IRB Approval

In this blog we cover how eConsent benefits trials and aligns with IRB ethical commitments, how to prepare...

Unlocking the power of Real-World Evidence in FDA submissions

An avalanche of data from so many real-world sources is available today, with the promise of more data...

21 November 2022

AKRN optimizes patient assessment collection with Castor ePRO

Castor's ePRO solution enabled AKRN and Company Z to engage with a participant population that, on their own,...

16 November 2022

How EDCs are Changing the Game in Clinical Research

An electronic data capture (EDC) system is software used to collect, clean, transfer, process, and store data in...

12 October 2022

AKRN creates the ideal case report form using Castor EDC

Learn how AKRN and Company Y were able to complete their 100-person study in nine months to help...

22 September 2022

AKRN handles mid-study changes in medical device clinical trials with Castor EDC

AKRN Scientific Consulting, a medical device CRO, used Castor's flexible EDC solution to handle constant mid-study changes for...

9 September 2022

5 steps for patient engagement and better outcomes in decentralized clinical trials

For successful decentralized clinical trials, researchers must encourage patient engagement. Learn 5 steps that modern companies are taking...

Automated data capture with eSource to train an AI algorithm

Castor’s eSource platform streamlined collecting, capturing & processing large amounts of clinical data to train AusculThing’s AI algorithm.

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