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Clinical trials and Research Blog
The Citruslabs blog covers all things clinical trial patient recruitment and retention as well as exciting news and developments in the medical research industry. Browse our recent posts or search for a topic you're interested in to learn more.
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Real-World Data vs. Real-World Evidence: Understanding the Difference
Real-world data and real-world evidence come up constantly in conversations about product validation, clinical studies, and regulatory strategy. They sound similar, and they are closely related, but they are not interchangeable. Understanding the difference matters if you are deciding how to support a product claim, design a study, or communicate credibility to regulators, partners, or consumers. This article explains what each term means, how they connect, and when brands ac
Ben Brockman
Jan 233 min read


What Is a Medical Device CRO and When Should You Use One?
If you are developing a medical device, you will eventually face the same question most teams do. How do you generate credible clinical evidence without slowing down development or overloading your internal team? A medical device CRO can help bridge that gap. This article explains what a medical device CRO is, what they actually do, and how to decide if working with one makes sense for your product and stage. A medical device CRO is a contract research organization that desi
Ben Brockman
Jan 214 min read


How to Avoid Participant Dropouts in Clinical Trials
Participant dropouts are one of the most common and costly challenges in clinical trials. When participants leave a study early, timelines slip, data quality suffers, and results can become harder to interpret. Dropouts in clinical trials happen when participants discontinue a study before completion, often due to burden, confusion, lack of engagement, or unmet expectations. You can reduce dropouts by designing participant-friendly protocols, setting clear expectations, maint
Ben Brockman
Jan 193 min read


Centralized vs. Decentralized Clinical Trials
Clinical trials are no longer just for pharmaceuticals. Today, health, wellness, and CPG brands rely on clinical research to validate product performance, support marketing claims, and build consumer trust. As research methods evolve, brands are increasingly choosing between centralized clinical trials, decentralized clinical trials, or a mix of both. Understanding the difference matters because the trial model you choose affects cost, timelines, participant diversity, and th
Ben Brockman
Jan 164 min read


What Are Adverse Events in Clinical Trials?
When conducting clinical trials, especially in the health and wellness space, it's vital to understand the concept of an "adverse event." These occurrences play a crucial role in trial evaluations, regulatory compliance, and the overall credibility of your brand. Whether you're testing a new skincare product, dietary supplement, or pet health solution, understanding adverse events can help you navigate clinical trials successfully. What Is an Adverse Event in Clinical Trials?
Ben Brockman
Jan 143 min read
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