CLP Rev. 9 — 1 November 2026: new hazard classes (endocrine disruptor, PMT, vPvM) apply to substances on the market. Is your SDS library ready?
001 — COMPLIANCE & DOCUMENTATION FOR FLAVOUR HOUSES

The compliance platform built for flavour houses.

Generate EU and FDA Safety and Technical Data Sheets — plus the full set of customer declarations — from a single formula. Audit every ingredient against the EU 1334/2008 positive list, with a deterministic 16-section REACH Annex II audit and ISO 9001 document control built in. Created by a flavour industry veteran with 25+ years' experience.

FIG. 01 / DOCUMENT GENERATION ONE FORMULA → FULL SET
INPUT PROCESS OUTPUT FLAVOUR FORMULA REF / FF-2406-OR-LMN INGR 01▓▓▓▓▓ INGR 02▓▓▓ INGR 03▓▓▓▓▓▓ INGR 04▓▓ INGR 05▓▓▓▓ INGR 06▓▓▓ INGR 07▓▓▓▓▓ PROPRIETARY SECURE PROCESSING ‹parse› ‹classify› ‹evaluate› ‹generate› ‹discard› SDS SAFETY DATA SHEET OK ALLERGEN DECL. HALAL CERT. TECH PACK SIGNED YOUR FORMULA · NEVER STORED · NEVER TRAINED ON
16-sectionREACH Annex II audit
EU 1334/2008Article 16 auditor
Full setdocuments per formula
0%used to train AI
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How it works.

FIG. 02 — PIPELINE

No setup project and no consultants. Upload a formula; Binacru enriches the data, applies the regulatory rules deterministically, and returns a full, audited document set you approve and issue under version control.

STEP 01

Upload your formula

Ingredients, codes and CAS, extracted automatically

Drop a formulation PDF or enter ingredients directly. Binacru reads the codes, percentages and CAS numbers. Your uploaded formula is processed and not retained, and never used to train AI models.

INPUT / PDF or directDATA / Discarded
STEP 02

Enriched by AI, classified by rules

The hazard maths is deterministic, never inferred

Ingredient data is enriched from PubChem and your own database. Mixture ATE, transport classification, signal words and H-codes are calculated by a rule-based engine — AI never touches the regulatory classification.

HAZARD / DeterministicAI / Data only
STEP 03

Audit, approve, issue

Checked against all 16 REACH Annex II sections

Every SDS is audited against the full Annex II structure before issue. Approved documents move through a Draft → Approved → Issued → Superseded lifecycle with named approvers and complete version history.

AUDIT / 16 sectionsCONTROL / ISO 9001
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One formula in. The full document set out.

FIG. 03 — OUTPUTS

The documents your customers and regulators ask for — and the declarations that usually mean another round of manual compiling — produced in a single pass.

DocumentTodayWith Binacru
01 Safety Data Sheet — SDS (EU & FDA) Authored by hand, 4–8 hrs Generated & 16-section audited
02 Technical Data Sheet — TDS (EU & FDA) Compiled manually Generated from your data
03 Allergen declaration (EU 14 / FDA) Cross-checked by hand Included in the set
04 Kosher & Halal self-statements Drafted per request Included in the set
05 GMO, Vegan / Vegetarian & Naturalness Drafted per request Included in the set
06 Labelling legal declaration Manual Included in the set

An outsourced SDS typically costs €200–500, and authoring one by hand takes a specialist 4–8 hours. Binacru produces the full set from a single formula.

Each statement is generated from your ingredient data and issued as your company's declaration — you keep final sign-off on accuracy.

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Built for flavour law, not just chemical safety.

FIG. 04 — EU 1334/2008

Green, yellow or red — on every ingredient, before formulation.

Enter the ingredient, CAS, FEMA, FL number, natural claim, botanical source and supplier. The Auditor checks the EU positive list (Annex I of Regulation 1334/2008), screens a contested-substance database (coumarin, estragole, pulegone, methyl eugenol), and adjudicates the natural claim under Article 16 — flavouring substance versus preparation versus "from a named food source".

A source on your Trusted Supplier list short-circuits to a verdict without a process-flow description. Every verdict is logged with findings, regulatory citations and action points — a full audit trail for ISO 9001 review.

Live verdict exampleEC 1334/2008
Vanillin, naturalCAS 121-33-5
Green
CoumarinCAS 91-64-5
Yellow
Estragole, isolatedCAS 140-67-0
Red
Orange Oil CPTrusted supplier
Green
Illustrative. Real verdicts include detailed findings, regulatory citations and action points.
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A platform, not just a generator.

FIG. 05 — CONTROL
AUDIT

Deterministic self-audit

Every SDS is checked against all 16 REACH Annex II sections by a rule-based engine: signal-word consistency, PBT/vPvB screening, SVHC disclosure, REACH Annex XIV checks, Section 14 transport, and Article 31(9) redistribution flags. No black box.

METHOD / Rule-basedSCOPE / 16 sections
CONTROL

ISO 9001 control — documents that stay current

Draft → Approved → Issued → Superseded with named approvers, version history, archived PDFs, Article 36 ten-year retention and automatic GHS five-year review alerts. As CLP and EFSA rules change — including CLP Rev. 9 — your library is brought current, not left to age.

STANDARD / §7.5.2REVIEW / Automatic
GLOBAL

Built for international houses

Multi-tenant isolation keeps every company's data separate. EU and FDA regulatory tracks, a four-language interface (English, Spanish, Turkish, Chinese Simplified), and a supplier-document auditor that reviews incoming TDS and SDS for red flags.

MARKETS / EU · FDAUI / EN·ES·TR·ZH

Binacru's regulatory frameworks track the standards monitored by EFFA and its national associations — including AEFAA in Spain — across EC 1334/2008, GHS/CLP, REACH and FEMA GRAS.

And it's fast — which is the quiet part.

Documents that took hours arrive in minutes. The point isn't speed for its own sake: it frees your regulatory time, and it means specs, quotes and samples reach your customers sooner.

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The whole compliance job, in one place.

FIG. 06 — WHAT IT CHANGES

From the formula on the bench to the document in your customer's inbox — defensible, auditable, and done in a single pass.

01 /

Compliant documentation and defensible natural claims without a regulatory headcount you can't yet justify — and quicker turnaround to your customers as a result.

02 /

More output, not more hours. Deterministic, auditable and regulator-ready — with final sign-off always staying with your team.

03 /

The hazard work done right. CLP mixture ATE, transport classification, the 16-section audit and contested-substance screening — with no AI on the classification.

One platform for the whole job — not a generic tool with "flavour" stickered on top.

007 /

Built from inside the industry.

FIG. 07 — FOUNDER

Binacru is built by Sebastian Iaconis25+ years in the flavour industry, across European and international markets, from bench formulation and emulsion work to regulatory affairs and technical presentations.

Plenty of tools exist for chemical safety. None of them know what EC 1334/2008 is, adjudicate an Article 16 natural claim, or understand FEMA GRAS and FL numbers. The large houses built this capability internally; everyone else still works in spreadsheets and Word templates. Binacru is the tool that gap needed — deterministic where the regulation demands it, AI-assisted where it saves hours, auditable everywhere.

"I spent years watching a regulatory officer lose a day to a single safety data sheet, and a flavourist defend a 'natural' claim on nothing but a supplier's word. Binacru is the tool I wished existed."
Profile / 001BINACRU
RoleFounder, Binacru
Experience25+ years, flavour industry
FocusRegulatory · formulation
BaseMurcia, Spain
LanguagesEN · ES · IT
MarketsEU · FDA · international
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See it on your own formula.

FIG. 08 — PROOF OF VALUE

Your data, your documents. Then decide.

Rather than a self-service trial, we run a Proof of Value. Sign a mutual NDA, send one anonymised formula, and on a 45-minute working call we generate a live EU + FDA TDS, a full 16-section SDS and the declaration set — from your own data, not a sample.

If it earns a deeper look, a 60-day paid pilot on your real data credits in full toward year one. No platform lock-in, no long commitment on day one.

Founding-customer terms

The first houses to come on board receive founding-customer pricing in exchange for a reference and a short case study. You get a lasting pricing advantage; we get the social proof. Time-bound, not permanent.

Proof of Value NDA-backed
FormatMutual NDA, then live session
Duration45 minutes
You bringOne anonymised formula (raw materials list)
You seeTDS + SDS + declarations, from your data
Pilot60 days, real data, credited to year 1
CommitmentNone to start
009 /

Questions, answered.

FIG. 09 — FAQ
What makes Binacru different from a general EHS or SDS platform?
Binacru is built only for the flavour industry. It enforces EU Regulation 1334/2008 positive-list compliance, adjudicates Article 16 natural flavouring claims, tracks FEMA GRAS status and handles FL numbers — none of which generic EHS platforms address. It also runs a deterministic 16-section REACH Annex II SDS audit with no AI involvement in hazard classification.
How does the Ingredient Auditor handle natural flavouring claims?
It accepts the ingredient, CAS, FEMA, FL number, natural claim flag, botanical source, process and supplier; cross-references the EU positive list and a contested-substance database; and applies Article 16 of EC 1334/2008 to adjudicate the claim — returning a Green, Yellow or Red verdict with findings, before the ingredient enters formulation.
Is the SDS hazard classification AI-generated?
No. The hazard maths is deterministic and rule-based: CLP mixture Acute Toxicity Estimates, transport classification, GHS signal-word logic and an H-code lookup table. AI is used only for data enrichment and drafting, never for regulatory classification — and every SDS is checked by a 16-section REACH Annex II self-audit before issue.
Does Binacru support ISO 9001 document control?
Yes. A Draft → Approved → Issued → Superseded lifecycle is built in with named approvers, version numbers, archived PDF snapshots, REACH Article 31(9) redistribution tracking and Article 36 ten-year retention — directly addressing ISO 9001 §7.5.2 (Control of Documented Information).
What about the new CLP Rev. 9 hazard classes?
CLP Delegated Regulation 2023/707 adds hazard classes for endocrine disruptors, PMT and vPvM. These apply to substances placed on the market from 1 November 2026. Binacru's H-code mapping and audit engine include the new classes, and your existing library is brought current rather than left to age.
Does Binacru support both EU and FDA compliance?
Yes. It generates documentation compliant with EU Regulation 1334/2008, EFSA standards and GHS/CLP/REACH, as well as FEMA GRAS and FDA requirements — from a single platform, with a default regulatory region per company that is switchable per document.
Where does my data live, and is it used for training?
Your uploaded formula is processed and not retained, your data is never used to train AI models, and each company's data is fully isolated — its own ingredient database and document library, on professionally managed cloud infrastructure in Europe with encryption and firewall-restricted internal services. A Data Privacy & Security Statement and a Mutual NDA are available on request.
How do I evaluate Binacru before committing?
Through a Proof of Value rather than a self-service trial. Sign a mutual NDA, send one anonymised formula, and on a 45-minute working call we generate a live EU + FDA TDS, a full 16-section SDS and the declaration set from your own data — so you see it handle your regulatory reality, not sample ingredients.
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Request a Proof of Value.

FIG. 10 — CONTACT

A live session on your own data.

Tell us what your team spends most time on today — SDS, TDS, the declaration set, or defending natural claims — and we'll show Binacru handle it on one of your formulas, under NDA.

Request a confidential demo

Your data is never shared or sold. A Mutual NDA is available on request before any technical discussion. Or email info@binacru.com.