AI-Powered Compliance Intelligence

Substantiate Your Supplement Claims in Minutes, Not Months

Stop spending hundreds of hours searching clinical trials, analysing studies, and drafting substantiation memos. Nutra Comp automates the entire process — from PubMed search to FDA-compliant claims — so you can launch faster.

No spam. Get early access and product updates only.

Nutra Comp report showing NAC clinical trials with human trial data, study details, dosage information, and significant findings

How It Works

From Ingredient to Substantiation in Four Steps

What used to take months of manual research now happens in minutes.

1

Search

Enter your ingredient and Nutra Comp searches PubMed for relevant clinical trials — RCTs, meta-analyses, and systematic reviews on healthy human subjects.

2

Analyse

AI reviews each study for oral administration, subject health status, significance of findings, and extracts p-values, effect sizes, and conclusions.

3

Generate

Automatically produces FDA-compliant structure–function claims ranked by evidence strength, plus a complete substantiation memo ready for review.

4

Export

Download your clinical evidence report, claims, and substantiation memo as polished, print-ready PDFs to share with your legal and compliance teams.

Features

Everything You Need to Substantiate with Confidence

Built for supplement brand owners who need rigorous, compliant evidence — without the compliance consultants.

PubMed Clinical Trial Search

Automated, exhaustive search of PubMed for RCTs, meta-analyses, and systematic reviews on healthy human subjects with oral administration.

AI-Powered Evidence Analysis

Intelligent extraction of p-values, effect sizes, study populations, and significance levels — distinguishing across-group from within-group findings.

FDA-Compliant Claim Generation

Structure–function claims generated in strict compliance with FDA, Amazon, and Google Merchant Center requirements. No disease claims, ever.

Substantiation Memo Builder

Produces a comprehensive substantiation memo with confidence scores, evidence tables, and mechanism-of-action data — ready for internal review.

One-Click PDF Export

Export your entire clinical evidence report, generated claims, and substantiation memo as professional, print-ready PDF documents.

Brand Profile Management

Save your brand details, ingredient lists, and past reports in one place. Revisit and update substantiation as new research emerges.

Pricing

Simple, Transparent Pricing

Choose the plan that fits your portfolio. All plans include full substantiation reports and compliance-ready documentation.

Standard

5 ingredient searches/month

$499/month
  • 5 ingredient searches per month
  • Full clinical evidence reports
  • Structure–function claim generation
  • Substantiation memo generation
  • PDF export
Join the Waitlist
Most Popular

Pro

25 ingredient searches/month

$999/month
  • 25 ingredient searches per month
  • Full clinical evidence reports
  • Structure–function claim generation
  • Substantiation memo generation
  • PDF export
  • Priority processing
Join the Waitlist

Enterprise

Unlimited ingredient searches/month

$5,000/month
  • Unlimited ingredient searches
  • Full clinical evidence reports
  • Structure–function claim generation
  • Substantiation memo generation
  • PDF export
  • Priority processing
  • Dedicated support
Join the Waitlist

FAQ

Frequently Asked Questions

Everything you need to know about Nutra Comp and supplement substantiation.

Substantiation is the process of gathering and documenting scientific evidence that supports the health claims you make on your supplement labels and marketing materials. The FDA requires that all structure–function claims be truthful, non-misleading, and substantiated by competent and reliable scientific evidence — typically clinical trials on healthy human subjects.

Nutra Comp searches PubMed for clinical trials relevant to your ingredient, filters for studies on healthy human subjects with oral administration, and uses AI to extract key data: p-values, effect sizes, study design, population details, and conclusions. It distinguishes between across-group and within-group significance and ranks evidence strength with a confidence scoring system.

Nutra Comp primarily searches PubMed/MEDLINE, the world's largest biomedical literature database maintained by the U.S. National Library of Medicine. We focus on peer-reviewed clinical trials, randomised controlled trials (RCTs), meta-analyses, and systematic reviews.

Yes. Nutra Comp generates structure–function claims in strict accordance with the FDA Small Entity Compliance Guide. All claims avoid explicit and implicit disease references. However, we recommend having your legal/regulatory team review the final output before use, as Nutra Comp is a tool to assist — not replace — professional compliance review.

Most ingredient searches complete within 5–15 minutes, depending on the volume of clinical literature available. Compare this to the typical manual process which can take 40–100+ hours per ingredient when done by a human compliance expert.

Absolutely. All clinical evidence reports, structure–function claims, and substantiation memos can be exported as professional PDF documents. These are formatted for easy sharing with your legal team, regulatory reviewers, or business partners.

Each search is one ingredient analysis — for example, searching 'Ashwagandha' or 'Vitamin D3'. The search generates a complete evidence report, claims, and substantiation memo for that ingredient. Your monthly allowance resets on your billing date.

We're currently in private beta. Join the waitlist to get early access and be notified when we launch. Early waitlist members will receive priority access and special launch pricing.