Question 1

Does ClaimsText replace a regulatory consultant?

Accepted Answer

No. It does the search, the extraction and the disease-claim screen, and writes down what it did and how far it got. Deciding which claims to make, and signing the memo, stays with the person responsible. Many of the people it is built for are consultants running it for their clients.

Question 2

Whose name is on the memo?

Accepted Answer

Whoever reviews and signs it. Each report carries its own brand name, responsible person and compliance officer, set before signing, and the memo prints all three. A consultant can run reports for several client brands from one account, with their own name as the compliance officer on each.

Question 3

How does ClaimsText analyse the evidence?

Accepted Answer

ClaimsText searches PubMed for clinical trials on your ingredient, records how many matched and how many it read, and extracts what each study measured: design, population, dose, p-values and effect sizes. It keeps the findings that went against the ingredient as well as the ones in its favour, distinguishes across-group from within-group significance, checks the studied dose against the dose your product delivers, and scores confidence on eight named components with the reasoning written out.

Question 4

Are the generated claims FDA-compliant?

Accepted Answer

Every claim is drafted as a structure–function claim and then screened, one criterion at a time, against the ten disease-claim criteria in 21 CFR 101.93(g)(2). The report shows each verdict and the wording that triggered it, so a reviewer can see why a claim passed rather than take it on trust. ClaimsText assists professional review; it does not replace it. The responsible person named in the memo makes the final call and signs it.

Question 5

What does it say when it could not read everything?

Accepted Answer

The counts. Each search records how many records matched and how many were retrieved, and a capped search is reported as capped. Where something could not be assessed, the memo says “not assessed” rather than staying silent, because silence in a signed document reads as assurance.

Question 6

What data sources does ClaimsText use?

Accepted Answer

PubMed/MEDLINE, and our internal database of PubMed studies already analysed for earlier reports, re-extracted whenever that analysis is out of date. Peer-reviewed human trials: randomised controlled trials, meta-analyses and systematic reviews. The report lists the search terms and the counts it used.

Question 7

What happens to a client’s formulation?

Accepted Answer

It is used to produce the report and for nothing else on our side. We do not sell it, and our AI providers are chosen on data-processing terms that exclude training on it. The privacy policy names the processors involved and how long data is kept.

Question 8

How long does a report take?

Accepted Answer

Five to fifteen minutes to produce, depending on how much literature there is. Reviewing it takes as long as a review should; the point is that the search, extraction and screen are written down, not that they were quick.

Question 9

Can I export my reports?

Accepted Answer

Yes. Both documents, the clinical evidence report and the substantiation memo, export as PDF, formatted for a regulatory file or a client deliverable.

Question 10

What does ‘reports a month’ mean?

Accepted Answer

Each report is one ingredient: the complete evidence report, the screened claims and the substantiation memo for that ingredient. Your monthly allowance resets on your billing date.

Question 11

Can I see a report before I pay?

Accepted Answer

Yes. The sample report is a complete ashwagandha report, run by ClaimsText’s founder for his own supplement brand, BioStack Labs, with nothing edited out. For your own product, LabelScan at labelscan.claimstext.com checks the label against 21 CFR 101 free and emails the findings; choose a plan when you want full reports on your ingredients.

Question 12

What is supplement substantiation?

Accepted Answer

Substantiation is the evidence behind a health claim on a supplement label or in its marketing. The FDA requires structure–function claims to be truthful, non-misleading and substantiated by competent and reliable scientific evidence, and the FTC applies the same standard to advertising. In practice that means human clinical trials, read in full, including the ones that went the other way.

What Is In Vitro Study?

Why It Matters for Supplement Brands

How It Works

Common Mistakes to Avoid

Related Terms

See It in Action

Automate Your Substantiation