Clinical Trials for Food Supplements

From protocol design and clinical trial conduct to data analysis and regulatory-standard clinical trial reports, the Functional Gut Clinic delivers end-to-end clinical trials tailored to your medicines and medical devices
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Our team brings considerable scientific expertise in designing efficient, cost-effective studies with focused, robust endpoints—ensuring your research meets the highest standards.
Speak to our clinical team within 2 business days

GI-specialist study design
Existing partnerships with other key opinion leaders
End-to-end trial management
Fast recruitment and high retention rate
Gold-standard GI testing and clinical assessments
Access to advanced biomarkers
Expert interpretation and analysis of data
Publication support
Generic study templates
Limited GI expertise
No biomarker integration
No claims guidance
Slower recruitment
No HCP interpretation

Live microorganisms with proven health benefits.
Non-digestible compounds that promote beneficial bacteria growth.
Products aimed at improving digestion and nutrient absorption.
Bioactive compounds or nutraceuticals targeting intestinal permeability.
Herbal, enzyme or adsorbent-based products for symptom relief.
Fibre blends, osmotic agents, or natural laxatives.
Supplements designed to reduce exercise-induced gastrointestinal symptoms.
Alginates, buffering agents or other indigestion remedies.
Multivitamins and other supplements designed to support your immune system.
A clinical trial for a food supplement or digestive health product is a structured study designed to evaluate how your product performs in real people under controlled conditions. Outcomes measured typically include reductions in bloating, improvements in bowel regularity, microbiome balance, intestinal permeability, and overall quality of life.

Credibility sells: in a crowded market, consumers and retailers choose products backed by real clinical evidence that help differentiate you from the competition.
Regulatory alignment: UK advertising standards require all health claims to be backed by evidence.

We can take your product through the entire research cycle, from protocol design and clinical trial conduct to data analysis and regulatory-standard clinical trial reports. We deliver end-to-end clinical trials tailored to you.
We offer a wide range of investigations and assessments, novel technologies, advanced biomarkers and validated questionnaires to demonstrate the safety and efficacy of your product.
Our extensive participant databases and advanced recruitment strategies enable us to identify and enrol eligible candidates faster than traditional methods. This streamlined approach not only accelerates study timelines but also ensures targeted participant selection. As a result, we consistently achieve above-average retention rates and deliver reliable, compliant data.
Our specialists ensure trials deliver high-quality, clinically relevant outcomes that make for highly publishable research.
Stool microbiome assessments
Gut permeability testing
Small intestinal bacterial overgrowth tests
Intestinal transit studies
Hydrogen sulphide assessment
Intestinal methanogenic overgrowth assessment
Carbohydrate malabsorption testing
Oesophageal manometry
24-hour reflux test
Gastric emptying test
Validated clinical outcome assessments
Patient-reported outcome assessments (ePRO, eCoA)
Quality of life assessments
Safety assessments
Biochemistry and haematology
Digital biomarkers
Nutritional biomarkers
Lifestyle questionnaires
Patient satisfaction
Anthropometrics
From study design to patient recruitment can take less than 3 months, depending on the complexity of the study and whether regulatory agency approval is required.
The size, duration and complexity of a study will determine its cost. The FGC offers industry-competitive costs with streamlined, efficient clinical operations.
FGC offers end-to-end clinical trial services, including study design and protocol authoring, site setup and recruitment, data management and analysis, study report and publication authoring.
FGC has three fully operational clinical sites located in London, Cambridge and Manchester, with the facility to work with other satellite and NHS sites as required.
That’s what we’re best at. Our team has experience in different trial designs and outcome measures to showcase your product.
It’s good practice to publish results of findings in peer reviewed journals, conference abstracts or on a clinical trials database. However, your results belong to your company, we can advise on how best to publicise them and take you through the whole process.