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Relay X

Anticipate regulation.

§ 01 — Your products
Your products,
in constant motion.
New version, new batch, new market: every change restarts a regulatory verification cycle.
§ 02 — The challenge
One single
regulatory truth.
Every framework, every text, every threshold — read, cross-checked and verified by AI continuously. All jurisdictions, all markets, in real-time.
§ 03 — The system
The OS of compliance.
AI agents verify compliance, track regulation, anticipate its evolution. To accelerate your time-to-market — without conceding on rigor.
The promise

One system to read, verify, write and anticipate. At the speed of real regulation.

Relay X live demo with cosmetics brands at a trade event
An ecosystem of trust
The problem

A regulatory dossier
takes weeks.

A Relay X agent handles it
in minutes.

Verification

Your ingredients,
compliant in every market.

Product context is understood: category, use, target markets. Every ingredient is checked in real time against the applicable framework: cosmetic INCI, food additives, REACH substances or pharmaceutical excipients. Upcoming changes are tracked continuously.

  • Semantic analysis: category, use, markets
  • Edge cases: thresholds, annexes, restrictions
  • Anticipation: regulatory revisions in progress

Anti-aging face cream

INCI% INCI
AQUA52.07%
HOMOSALATE8.00%
BENZOPHENONE-34.00%
GLYCERIN4.98%
CETEARYL ALCOHOL3.50%
PHENOXYETHANOL0.95%
LINALOOL0.12%
LINALOOL at 0.12 %: fragrance allergen, individual declaration mandatory in INCI list (Annex III · Reg. (EU) 1223/2009).
Supplier documents

Every supplier dossier,put through the screen.

Raw materials, technical files, attestations, certificates: any document, from your PIM/PLM/ERP or dropped directly.

Relay X extracts, verifies against your checklists and compares.

A shared workspace for your teams and your suppliers. No more email threads, no more lost versions.

Raw material approvalLive
Drop in an SDS, COA, or supplier attestation
Export
Global monitoringLIVE · continuous feed

Regulation,
monitored in real time.

Authorities, scientific committees, industry bodies: EUR-Lex, ECHA, FDA, EMA, NMPA, ANVISA, EFSA, and dozens more. Every change is assessed for its impact, product by product.

And beyondScientificCompetitiveSector
Live
Global
Targeted
Active regulatory hubWeak signal detectedScroll to explore
Your productsLabels & packagingGlobal markets

Every package,
seen from every angle.

Dossiers, spreadsheets, charts,
ready for the authority.

PIF · spreadsheets · chartsextraction · comparison · sourced & verified
PIF · Renewing serum 30 ml
§ 3.2

§ 3.2 · Overall toxicological profile. Raw materials assessed in accordance with Annex I, point 8 of Regulation (EC) No 1223/2009. No ingredient classified as CMR 1A/1B under the CLP Regulation.

Retinol (0.3% RE) concentration complies with Regulation (EU) 2024/996, applicable to placements on the market since 01.11.2025.

§ 2.1 · ChartQuality monitoring · 3 months
25 °C40 °C · accelerated aging
Template · RelayX-PIF-v312 sections · 4 spreadsheets · 3 charts
The acceleration

Faster,
and sharper.

Every day saved,
is market won.

Voices

In their
own words.

Regulatory Affairs Director
The time we used to spend on regulatory verification has shrunk dramatically. Our launches are no longer held back by compliance, and we hit our market windows without conceding on rigor.
M. R.European cosmetics group
Raw Materials Lead
Raw material approval has become a fluid process. Extracting and verifying supplier dossiers no longer costs us weeks of back-and-forth, and traceability holds up from first document to last.
C. L.Cosmetics manufacturer
Laboratory Director
Maintaining our accreditations demands constant documentary rigor. Relay X keeps our procedures aligned with every normative shift. We now approach every audit with composure.
Dr. P.Independent analytical laboratory
R&D Director
We innovate knowing what will pass, and on which markets. No more late-stage surprises. That visibility changes the very nature of our product trade-offs.
S. M.Premium skincare brand
Founder, regulatory consultancy
My clients expect coverage across ever more jurisdictions, and regulatory pressure keeps rising. My team absorbs the load without diluting the quality of our recommendations.
F. T.Regulatory affairs consultancy
Infrastructure

Sovereign hosting on OVH.

Your data is stored in France, on OVH infrastructure. No transfer outside the EU, no training on your content, strict per-client isolation.

Paris · GravelinesDatacentersAES-256 · TLS 1.3EncryptionGDPRCompliance
Governance

Human-in-the-loop & traceability.

Every response is sourced, timestamped, auditable. The agent proposes and justifies. Your regulatory affairs team decides.

Deployment

Instant deployment.

Tailored to your organization in two weeks maximum. We shape the solution to your processes, checklists, and reference frameworks, not the other way around.

Demo

See.
Understand.
Decide.

A live demo on your products, your markets, your constraints. We come with answers, not slides.

Mathis GinesteBook a slotStraight into Mathis’ calendar · CEO

Instant confirmation · Data processed per GDPR

Relay X · AI Operating System for Compliance