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ePRO and Cancer Research: Measuring the true patient experience
In this on-demand webinar, we delve into the nuances of measuring true QOL & PRO for oncology trials.
The impact of ePRO on the patient & site journeys
Watch the recording of our product webinar on the impact of electronic Patient Reported Outcomes (ePRO) from two...
The Place of COAs / PROs in the Future of Healthcare
Learn how integrating Patient-Reported Outcomes (PROs) into clinical trials can drive success in Value-Based Care (VBC).
From Paper to eCOA / ePRO: Bringing flexibility & efficiency to your clinical trials
In this on demand webinar discover if your protocol is a good candidate for eCOA / ePRO, and...
Kicking-off 2024: A year of optimism & opportunity
Listen in for Derk’s take on the JPM conference, and what to expect from a first quarter filled...
Product Spotlight: Castor ePRO
In this on-demand webinar we dive into the benefits and capabilities of ePRO, and how Castor’s web and...
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...
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,...
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...
Electronic Case Report Forms (eCRFs) in Clinical Trials: Shifting to a Modern Research Paradigm
Castor is shifting the research paradigm for eCRF in clinical trials, transitioning from old, inefficient processes to a...
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
Getting Started with DCT in 2022
Castor advisor Craig Lipset, suggests that you consider DCT technology as three separate tiers. Learn more about these...
How to Incorporate Remote Technology in Your Next Medical Device Trial
Researchers are looking to incorporate remote technologies into medical device trials for a wide range of device classifications....
Introducing Castor Connect
Watch this webinar for tips on how to ensure research continuity during COVID-19 by running your trial with...
PMCF & RWE: Roles of Medical Device Registry Studies & ePROs
Registry studies focused on a specific medical device are a valuable tool to capture the safety and outcomes...
A Guide to Capturing and Managing Data in Digital Therapeutics Trials
This playbook is a tool for sponsors and CROs who want to leverage DCT technology to support remote...
eBook: The Decentralized Clinical Trial Playbook
This playbook is a tool for sponsors and CROs who want to leverage DCT technology to support remote...
Electronic Patient Reported Outcome (ePRO) Measures: Questionnaires & More
Patient reported outcome measures in clinical trials have traditionally been done on paper. Surveys are a common way...
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