When brands talk about being clinically tested, the type of study behind that claim matters. One commonly used and often misunderstood research design is the open label study. Especially popular in supplements, skincare, cosmetics, superfoods, and pet health, an open label study offers valuable real-world insights, when designed and communicated correctly. In this post, we’ll break down what an open label study is, how it works, its benefits and limitations, and why it plays
False advertising is often discussed as a legal or ethical issue. But for brands, the bigger story is economic. Misleading or unsubstantiated claims can quietly drain revenue, inflate costs, and limit long-term growth, even when no lawsuit ever happens. This article explains the real financial impact of false advertising, how those costs show up across a business, and when investing in evidence can help brands avoid expensive mistakes. False advertising negatively impacts th
Choosing a Contract Research Organization is one of the most important decisions you make when running a clinical study. The right CRO does more than execute a protocol. They help you reduce risk, stay aligned, and generate evidence you can stand behind. This article explains how to build a strong, productive partnership with your CRO, from the first conversation through post-study collaboration, so your trial runs smoothly and delivers meaningful results. A strong partnershi
Collagen is one of the most popular ingredients in supplements, foods, and beauty products. But popularity alone does not build trust. Brands increasingly rely on collagen clinical studies to understand what collagen actually does in humans and how to communicate those findings responsibly. This article explains what collagen clinical studies are, what they typically measure, and how brands use them to support product development and marketing decisions. Collagen clinical stu
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
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
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
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
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?
You’ve poured months, maybe years, into developing a product you believe in, whether it’s a glow-boosting serum, a gut health supplement, or a mobility chew for senior dogs. Now comes the hard part: proving it works. In a crowded market full of unverified claims, one of the most powerful ways to stand out is through clinical evidence. That’s where the parallel group study comes in, a trusted research design that gives brands the data they need to validate product claims and w
Clinical trials are the gold standard for validating the safety and efficacy of skincare products and dietary supplements. Within this landscape, the crossover study design stands out for its unique ability to minimize variability and optimize study efficiency. In this blog post, we’ll explore what a crossover study is, how it works, and why it's particularly valuable for brands in the skincare and supplement industries. What is a Crossover Study? A crossover study is a type
Walk down any skincare aisle, and you’ll see the same buzzwords everywhere, “clinically tested,” “proven results,” “dermatologist-approved.” But with so many products making big promises, how do you know which ones actually deliver? That’s where dermatology clinical trials come in. These behind-the-scenes studies are the real reason some products earn trust while others fade fast. They’re how brands back up their claims and how consumers can feel confident that what you’re p
