Product compliance software

Product compliance software for EU and US documents

Doc2Shelf turns supplier documents into structured, review-ready GPSR safety content, DPP-oriented preparation data (structured JSON), and EU/US compliance declaration drafts — without re-entering the same product data for every document.

Free plan included — no credit card required.

Product compliance work often starts with the same facts scattered across spec sheets, safety data sheets, labelling guides, and supplier catalogs. Teams repeatedly copy those details into safety blocks, declarations, and traceability records, creating delays and inconsistent documents across a catalog.

Doc2Shelf extracts the product data once and uses it to draft the compliance output your workflow needs. You can review every field against the source document, resolve missing information, and export or publish only after a person has signed off.

How it works

  1. 1

    Upload supplier documents

    Add spec sheets, safety data sheets, labelling guides, or catalogs.

  2. 2

    Extract product data

    AI structures relevant facts and scores each extraction for confidence and completeness.

  3. 3

    Generate the required output

    Choose the applicable GPSR or EU/US declaration draft, or prepare DPP-oriented structured data for review.

  4. 4

    Review and export

    Resolve missing fields, verify the draft, and approve it before publishing or export.

One product record, several compliance documents

The same structured product record can feed GPSR manufacturer and product-identification details; responsible-person details when the manufacturer is not established in the EU; warning or safety information where applicable; DPP-oriented preparation data (structured JSON); and EU or US compliance declaration drafts. That shared source keeps identity, specifications, and safety details consistent across documents.

Each specialist workflow remains separate, so you can generate only the output relevant to the product and market instead of forcing every item through one generic template.

From supplier PDF to review-ready output

Doc2Shelf reads supplier PDFs, extracts compliance-relevant fields, scores each extraction for confidence and completeness, and flags required information it cannot determine. Extracted facts keep their source page and a short quote, and the generated content remains editable, making review faster without hiding uncertainty.

Use the finished product data in marketplace listings as well as compliance documents, so catalog and regulatory workflows start from the same reviewed facts.

Human review stays in control

Doc2Shelf drafts and structures documents; it does not assess conformity, certify products, or replace legal review. A review gate backed by content hashing prevents unreviewed compliance content from being published or exported.

That separation lets teams automate repetitive preparation while keeping responsibility for accuracy and approval with the people who know the product and its requirements.

Compliance documents by product category

Each product category brings its own EU and US rules, and each rule expects different information. The table summarizes the main legislation to consider for the seven categories Doc2Shelf supports and what its declaration drafts cover. It is a starting point, not a complete list: other rules may apply depending on the product, and some products fall under several categories.

On top of category rules, the EU General Product Safety Regulation (EU) 2023/988 acts as a safety net for consumer products — food is excluded from it — and its Article 19 sets the information online offers must show. For products outside the seven categories, a custom declaration lets you define the sections yourself.

EU and US rules to consider, by category
CategoryEU rules to considerUS rules to considerWhat Doc2Shelf drafts
FoodFood information to consumers, Regulation (EU) No 1169/2011FDA food labeling, 21 CFR Part 101Ingredients, allergens, nutrition, net quantity, business operator or manufacturer, origin, storage
CosmeticsRegulation (EC) No 1223/2009: Responsible Person, safety report, product information file, CPNP notification, label particularsMoCRA registration and listing; labeling under 21 CFR 701; warnings under 21 CFR 740INCI ingredients, nominal content, durability, precautions, responsible person, batch; US identity, ingredients, warnings
ElectronicsLVD 2014/35/EU, EMC 2014/30/EU, RED 2014/53/EU, RoHS 2011/65/EU; CE marking and EU declaration of conformityFCC rules (47 CFR Part 15) where applicable; a GCC where a CPSC rule appliesDeclaration of conformity content, directives, standards, CE, RoHS and WEEE information; FCC statements
ToysToy Safety Directive 2009/48/EC with EN 71 standards; Toy Safety Regulation (EU) 2025/2509 from 1 August 2030ASTM F963-23 (16 CFR 1250); Children’s Product Certificate with third-party testing; tracking labels; small-parts warningsDeclaration, standards, CE, age grading, warnings; US tracking label, choking-hazard warnings, testing details
ChemicalsREACH Article 31 safety data sheets (Annex II, Regulation (EU) 2020/878); CLP labelling, revised by Regulation (EU) 2024/2865OSHA Hazard Communication Standard, 29 CFR 1910.1200: safety data sheets and shipped-container labelsHazard identification, composition, signal word, hazard and precautionary statements, pictograms, first aid, supplier
TextilesTextile Labelling Regulation (EU) No 1007/2011; care labelling is not mandated EU-wideTextile Act rules (16 CFR 303), Wool Act rules (16 CFR 300), Care Labeling Rule (16 CFR 423)Fibre composition, care, size, origin, manufacturer; US fiber content, care, origin, RN
Food supplementsFood Supplements Directive 2002/46/EC: mandatory particulars and daily-portion declarationsSupplement Facts (21 CFR 101.36); structure/function disclaimer (21 CFR 101.93)Ingredients, nutrition, daily dose, warnings, storage; US Supplement Facts, suggested use, disclaimer

Centralizing compliance data across a catalog

Compliance data tends to live in many places: supplier PDFs in shared drives, warnings in a spreadsheet, importer details in an email thread. Doc2Shelf keeps it in one product record per item, built from the supplier documents, so every declaration draft, GPSR block and listing reads from the same reviewed values.

Supplier PDFs can be uploaded in batches of up to 500, within your plan’s document allowance. Each extraction carries a confidence score and a completeness score, and extracted facts are stored with the page and quote they came from.

What the product record holds
Data groupExample contentsUsed in
IdentityName, manufacturer, model number, category, GTIN, SKUListings, declarations, GPSR block
SpecificationsDimensions, ratings, materials, ingredients, nutrition valuesListings, category declarations
Compliance dataStandards, directives, certifications, markings, safety notesDeclaration drafts
GPSR dataManufacturer, importer, responsible person, distributor, warningsGPSR block, declaration contact sections
TraceabilityBatch or lot number, serial number, production date, country of originGPSR block, labels

Review gate and audit trail

Products, listings and declarations each have their own review gate. When a person approves an item, Doc2Shelf records who reviewed it, when, and a SHA-256 hash of the reviewed content. Publishing and export check that hash: if the content has changed since approval, the review is invalidated and the item has to be reviewed again before it can be used.

This gives a simple, verifiable link between what was approved and what was published or exported. It does not replace your own quality records — such as who decided a field did not apply and why — but it prevents unreviewed edits from slipping through.

Keeping documents current when rules or products change

Compliance documents age in two ways: the product changes (new supplier, new formulation, new warning), or the rules change. When a supplier sends an updated document, upload it, regenerate the affected drafts, and review them; editing reviewed content invalidates the earlier approval, so outdated approvals do not carry over.

Doc2Shelf does not monitor legislation for you. Your team decides when a rule change affects a product and then updates the record and drafts. Examples of recent and upcoming dates worth tracking:

Examples of rule changes that affect product documents
DateChangeAffects
8 July 2026CPSC eFiling of certificate data at entry (8 January 2027 for certain foreign-trade-zone products)US importers of products needing a GCC or CPC
31 July 2026End of placing on the market for cosmetics not meeting the expanded fragrance-allergen labelling (Regulation (EU) 2023/1545)EU cosmetics labels and ingredient lists
18 February 2027Battery passport required for EV, LMT and industrial batteries over 2 kWh (Regulation (EU) 2023/1542)EU battery documentation
1 January 2028CLP distance-sales and advertising label-element rules applyOnline offers for hazardous chemicals in the EU
1 August 2030Toy Safety Regulation (EU) 2025/2509 applies, with a digital product passport in place of the declaration of conformityEU toy documentation

Who uses product compliance software

Different teams use the same records for different jobs:

  • Compliance teams preparing declaration drafts and safety information for many products at once, with a review trail.
  • Importers collecting manufacturer, importer and responsible-person details from non-EU suppliers.
  • Brands with own-label products, which become the manufacturer under GPSR Article 13 and need consistent documents across ranges.
  • Marketplace and webshop sellers who need GPSR information and listing copy from the same reviewed data.
  • Distributors checking that the information they must verify is present before making products available.

Official sources and scope

Selected primary government and regulatory materials relevant to topics on this page.

These selected links are not exhaustive; category- and product-specific rules may also apply. Doc2Shelf structures review-ready drafts from supplied product data. It does not assess conformity, certify products, guarantee compliance, or replace legal or qualified technical review.

GPSR safety content

Draft manufacturer and product-identification fields, responsible-person details when the manufacturer is not established in the EU, and applicable warning or safety fields.

EU & US declarations

Generate editable, category-aware declaration drafts from reviewed product data.

DPP preparation data

Structure identity, materials, and compliance data into DPP-oriented preparation data (structured JSON).

Required-field prompts

Surface missing information before a document reaches review or export.

Source traceability

Record extracted facts with their source page and a short supporting quote.

Review gate

Require a person to approve generated content before it can be used.

Who it’s for

  • Compliance teams preparing documents across a large product catalog
  • Importers organizing supplier data for EU and US market requirements
  • Ecommerce teams aligning product listings with reviewed safety information
  • Distributors standardizing compliance-document preparation across suppliers

Frequently asked questions

What product compliance documents can Doc2Shelf generate?
Doc2Shelf can draft GPSR safety content and EU or US compliance declarations, and prepare DPP-oriented preparation data (structured JSON), from supplier documents. Available output depends on the product data and workflow you select.
Does Doc2Shelf certify that a product is compliant?
No. Doc2Shelf extracts data and generates review-ready document drafts; it does not assess conformity, certify products, or guarantee regulatory approval. You remain responsible for reviewing the content and meeting applicable requirements.
Can the same data be used in product listings?
Yes. The reviewed structured product record can feed Shopify and WooCommerce listings and prepare reviewable eBay-targeted draft copy for generic CSV/JSON export, reducing duplicate data entry between catalog and compliance workflows. The export is not an eBay import schema.
How is generated compliance content reviewed?
Each extraction carries a confidence and completeness score, extracted facts keep their source page and quote, required gaps are flagged, and a review gate prevents publishing or export until a person has approved the content.
Which product categories does Doc2Shelf cover?
Seven categories — food, cosmetics, electronics, toys, chemicals, textiles, and food supplements — each with an EU and a US declaration draft, plus a custom declaration whose sections you define.
Does Doc2Shelf track regulatory changes automatically?
No. Doc2Shelf does not monitor legislation. When your team decides a rule change affects a product, you update the product record, regenerate the drafts, and review them again.
What happens to an approval when someone edits reviewed content?
The review is invalidated. A hash of the reviewed content is stored at approval, and publishing or export is blocked until a person reviews the changed content again.
Can Doc2Shelf handle a whole catalog?
Yes. Supplier PDFs can be uploaded in batches of up to 500, within your plan’s document allowance, and each resulting product, listing, and declaration draft goes through the review gate.
  • What is a safety data sheet (SDS)?

    What a safety data sheet is, the 16 SDS sections, EU and US rules, SDS vs TDS, and which sections feed product listings and shipping data.

  • GPSR requirements for online sellers

    What the EU General Product Safety Regulation asks online sellers to show in product listings, with a practical checklist.

  • EU responsible person

    Who can act as the EU responsible person under GPSR and Regulation (EU) 2019/1020, what they must do, and where their details must appear.

  • CE marking explained

    What CE marking means, which products need it, self-declaration vs notified body, and the step-by-step process from legislation to affixing the mark.

  • EU declaration of conformity template

    The structure of an EU declaration of conformity, a fill-in template, and the mistakes that cause problems with authorities and marketplaces.

  • Digital Product Passport requirements

    What an EU Digital Product Passport is under ESPR, which products need one first, the 2024–2030 timeline, and how to prepare product data now.

  • EU cosmetics labelling requirements

    What a cosmetic label must show under Regulation (EC) No 1223/2009, how to write the INCI list, and the new fragrance-allergen dates.

  • Toy safety requirements in the EU and US

    EN 71 and the EU Toy Safety Directive, the new Toy Safety Regulation (EU) 2025/2509, and US CPSIA rules: ASTM F963-23, CPCs, testing and limits.

  • Textile labelling requirements (EU & US)

    Fibre names, composition percentages, tolerances, care labels, country of origin, and RN numbers under EU Regulation 1007/2011 and the FTC textile rules.

  • US certificates: GCC vs CPC and eFiling

    When a product needs a General Certificate of Conformity or a Children’s Product Certificate, the seven required elements, and how CPSC eFiling works.

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