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Oncology factsheet
Download our oncology factsheet to view an overview of our services.
Real-world evidence factsheet
Download our RWE factsheet to view an overview of our services.
How Advanced Neuromodulation Researchers Cut Study Build Time by 63% Using Integrated Trial Technology
This detailed case study reveals the practical strategies and technology solutions that enabled researchers to automate participant screening,...
Participant View eCOA | ePRO
Reduce participant and site burden with a simple 2 step onboarding and user-friendly app. Secure questionnaires via email...
eCOA/ePRO factsheet
Download our ePRO/eCOA factsheet to view an overview of our services.
Clinical Trials Aren’t Just About Patients (and That’s Okay)
This article explores the debate between patient-centricity and protocol-centricity in clinical trials, featuring insights from Derk Arts (Castor)...
Strategies to Minimize Participant and Healthcare Provider Burden in Clinical Trials
This article examines strategies to reduce participant and provider burden in clinical trials while ensuring high-quality data collection....
What do we measure with PROs in head and neck cancer? Pain, QoL, adverse events and more
Patient-Reported Outcomes (PROs) are essential in head and neck cancer research, offering insights into symptoms, quality of life,...
2024: Castor Year in Review
As we close the year, the Castor team shares vital milestones the company has achieved to make patient-centric...
A New Perspective on Clinical Research: Accessibility and Innovation
Joost Rigter’s inspiring journey highlights the importance of accessibility in clinical research. From AI-driven tools to simplified communication,...
Local Labs in the EDC: Streamlining Safety and Efficacy Insights
Local labs are a vital part of clinical trials, offering fast, cost-effective insights into safety and efficacy. But...
Beyond Compliance: How Quality Culture Drives Clinical Trial Excellence
Moving beyond compliance, quality culture drives clinical trial innovation through automated processes and measurable results.
eCOA Evolution: Have We Overcomplicated What Used to Work?
A blueprint for engineering elegant eCOA solutions that make complex trials feel simple.
Waiver of Consent vs Waiver of Written Consent
One is very common, the other is rarely granted. Learn the key differences between waiver of consent &...
Unlocking FDA’s Vision for PRO Collection in RWE: Timing, Methods, and Insights
Discover FDA's guidance on collecting PROs for Real-World Evidence (RWE), focusing on timing, methods, and improving data quality.
FDA’s Vision on PRO/eCOA Collection for RWE: Timing and Methods Explained
Watch back as our panel of experts discuss how the FDA views the collection of patient-reported outcomes for...
Understanding Phase 4 Clinical Trials: A Critical Component of Post-Marketing Insight to Drugs in the Real-World
When it comes to Phase 4 clinical trials, Castor's cutting-edge Real-World Evidence (RWE) platform is your key to...
Castor Launches “Castor for Impact Program” to Advance Health Equity in Clinical Research
Innovative Program Offers Discounted or Free Access to Clinical Trial Technology, Empowering Underserved Research Areas and Early-Stage Biotech...
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