Illustrated map of Europe connected with chemical documentation and compliance data

Chemical compliance across markets

Safety data sheets.
Clear compliance.
Every market.

Bring substance data and chemical documentation into controlled workflows that keep European and United States regulatory contexts separate.

16
structured SDS sections
8
market entry points
1
traceable workflow
Safety Data Sheets CLP classification UFI & PCN CAS substance data Controlled review

Start in the right place

Choose your market.

Each market has its own language, knowledge base and controlled publication status. Poland remains served by KartaCharakterystyki.com.

Each language area has its own publication status. Pages awaiting expert review remain excluded from indexing.

Expert-prepared documentation

Request a
Safety Data Sheet.

Provide your product composition and basic information. Our specialist will assess the formulation, calculate the applicable classification and prepare your Safety Data Sheet.

16 structured SDS sections 1 professional review PDF electronic delivery
Start your SDS request

Controlled intake

Tell us about
your formulation.

Missing test data will not block your request. We will mark gaps clearly and contact you before completing the document if additional evidence is needed.

01

Product details

Identify the product and the market where the document will be used.

Physical form*
The product is intended for*
02

Product composition

Add every substance and commercial raw material. Supplier documentation is particularly important for trade-name ingredients.

Example
Phosphoric acidCAS 7664-38-2 · EC 231-633-2 · 25%
WaterCAS 7732-18-5 · EC 231-791-2 · 74%
Corrosion inhibitorUnknown identifiers · 1%

Why supplier SDS files matter: a commercial raw-material name often does not disclose its complete composition or classification.

03

Product properties

Enter available measured values. Do not estimate values simply to complete the form.

04

Existing documentation

Upload the evidence that should be considered during assessment.

05

Company details

These details identify the requesting company and support preparation of Section 1.

06

Additional services

Select anything else your project may require. Options outside the standard scope are confirmed separately.

Scope and price

The stated price applies to a standard formulation containing up to 10 ingredients, provided that complete composition and current supplier documentation are supplied. Complex products, substances of unknown or variable composition, nanomaterials, biocidal products and formulations requiring additional regulatory or toxicological assessment may require an individual quotation. No additional work will be started without the customer’s approval.

Standard formulation€39.99 / $45.99Review precedes confirmation of scope.

One controlled environment

One platform.
Multiple markets.

CompliWorld is designed to connect regulatory evidence, formulation data and document content without treating translation as a substitute for compliance review.

See how the workflow fits together
01

Structured source data

Keep substance identifiers, concentration ranges, supplier information and decision inputs connected to the document.

02

Market-aware content

Separate language, market profile and publication status so teams know which version they are reviewing.

03

Traceable approvals

Make review status, changes and unresolved questions visible before a document reaches a customer.

From composition to controlled document

A workflow built around decisions.

Software should make the chain of evidence clearer, not hide it behind generated text.

  1. 01

    Collect

    Bring together product identity, intended use, formulation ranges and supplier source data.

  2. 02

    Assess

    Review CLP inputs, applicable concentration limits and the evidence behind each decision.

  3. 03

    Build

    Connect decisions across all sixteen SDS sections and the selected document language.

  4. 04

    Control

    Record status, expert questions, revisions and approval before controlled publication.

Designed around responsibility

Built for the people behind the product.

Different roles begin with different evidence, but all need a reliable route from product data to a controlled SDS.

Technology supported by chemical expertise

A platform should explain what still requires judgement.

“Our goal is not to replace responsibility with generated text. It is to make source data, decisions and unresolved questions easier to see and control.”

Paweł Jagieniak
Chemical technologist · Author and platform founder

Source-aware workflowsVisible review statusMarket-specific publication control

Begin with your market

Make the next compliance step clear.

Choose the right language platform or speak directly with us about your products and documentation workflow.