How quickly we recruit, how consistently people participate, and the community behind the work.
Book a 30-minute intro to talk through scope, timing, and the evidence your team needs.
Start with what you need to learn. Build the protocol, measurements, and analysis around that objective.
The endpoint, study design, and analysis plan set the boundaries for what the research can tell you.
Find your study approach →Protocol development, IRB submission, recruitment, participant support, and measurement in one coordinated research process.
Explore measurement →Reporting connects the results to your original objective, including what the evidence supports and where its limits lie.
See what you receive →Best for an early go / no-go decision. A pilot is not automatically designed to substantiate a product claim.
Explore the Pilot StudyBest for a defined evidence need. The design and findings determine which conclusions can be supported.
Explore Clinical ResearchThree parts of every study adapt to you: the design, the scope, and the timeline.
Real-world evidence or a randomized controlled trial. Longitudinal designs with rolling enrollment. Pre-trial and post-market surveillance. The format follows your business need.
Every study is scoped to your product, your claims, and your budget.
Studies are typically completed within 2 to 6 months, depending on recruitment complexity and intervention duration.
Wearables, surveys, validated instruments, biomarkers, labs, and specialized assessments.
Collection and lab measurements built around the study endpoint.
Validated surveys and participant-reported outcomes, personalized to your study. We can pull in different validated instruments and customize with visual analog scales. The list below is a starting set, and most surveys can be supported.
Clear, decision-ready evidence, delivered to the scope you agreed.
Objectives, methods, analysis, and findings in one clear record.
The agreed dataset and analysis, with the context to use them.
Findings translated for research, marketing, legal, and investor teams.
What the evidence supports, what it does not, and what remains unresolved.
Evidence to guide product, messaging, and market decisions.
Human evidence to inform formulation and commercial conversations.
You do not need a finished protocol to start the conversation.
No. A pilot can help explore an early signal. If you already have a defined objective and evidence need, a full study may be the better starting point.
The design, participant eligibility, sample size, measurements, study duration, and reporting scope. These are defined for your study rather than promised as a universal package.
That depends on the design and the findings. We begin with the objective you want to evaluate and explain the conclusions the resulting evidence can and cannot support. A positive finding is not guaranteed.
Your product or ingredient, the objective or claim you want to investigate, any existing evidence, and your timeline. A budget range is helpful, but you do not need to know the study design yet.
Bring your product, your question, and your timeline.
Let’s talk about the research that fits.