Health Claim Validation for FDA and EU Compliance

Reglyr checks every product claim against the EU Health Claims Register, FDA structure/function rules, and market-specific registers — showing exactly what is allowed, what requires substantiation, and what is prohibited.

Health Claim Validation
for FDA and EU Compliance

One Wrong Claim Can Delay Your Entire Launch

Most supplement and CPG brands discover non-compliant health claims at the worst possible moment: during retailer onboarding or regulatory review, weeks before a planned launch. Manually cross-referencing the EU Health Claims Register, FDA structure/function rules, and ASEAN/APAC market registers is slow, error-prone, and rarely scales across a portfolio. Reglyr maps each claim against every applicable market-specific register simultaneously, returning a clear verdict on whether a claim is permitted, requires substantiation, or is outright prohibited — before a single label goes to print.

Every Claim Checked Per Market

Claim by Claim Evaluation

Every Claim Checked Per Market

Reglyr evaluates each health or functional claim individually against the register that governs it in each target market — so you know exactly which claims are compliant, which need evidence, and which must be removed before launch.

  • Verdict per claim per market
  • Covers supplements and functional foods
  • No manual register cross-referencing
EU, FDA and APAC Registers

Multi-Register Coverage

EU, FDA and APAC Registers

Validation spans the EU Health Claims Register (EC 1924/2006), FDA structure/function claim rules, and ASEAN/APAC market-specific registers — in a single evaluation run, so teams targeting multiple regions see all gaps at once.

  • EU Health Claims Register covered
  • FDA structure/function rules applied
  • ASEAN and APAC registers included
Substantiation Required or Prohibited

Claim Classification

Substantiation Required or Prohibited

Not all non-compliant claims are equal. Reglyr distinguishes between claims that can be retained with proper scientific substantiation and those that are categorically prohibited, giving regulatory teams a prioritized action list rather than a generic flag.

  • Separates fixable from prohibited claims
  • Prioritized remediation action list
  • Reduces legal review cycle time
Prevent Costly Launch Delays

Launch Risk Reduction

Prevent Costly Launch Delays

Non-compliant claims are one of the most common causes of retailer rejection and regulatory hold-ups during market entry. By validating claims before label finalization, teams avoid reprints, reformulations, and missed retailer windows.

  • Catches issues before label print
  • Reduces retailer rejection risk
  • Validates ahead of market entry
Validate Claims Across Your Portfolio

Portfolio Scale

Validate Claims Across Your Portfolio

For CPG brands and consultancies managing multiple SKUs, Reglyr runs health claim validation across an entire product portfolio simultaneously — producing market-ready verdicts for every SKU without manual claim-by-claim review.

  • Scales across 10 to 200 plus SKUs
  • Consultancy multi-client workspace supported
  • Consistent verdicts across all markets

Validate Your Health Claims Before Launch

See how Reglyr checks your claims against the EU Health Claims Register, FDA rules, and APAC registers in a single run.

Book a Demo

Frequently Asked Questions