Reg (EU) 2024/2847Generate dossier — €149
LIVE — Enforcement tracker · Deadline dashboard · Transposition status — Updated weekly from EUR-Lex, Safety Gate, OEIL & 12 official sourcesView regulatory intelligence →

You manufacture products with digital elements outside the EU and sell them on the European market. Article 18 of Regulation (EU) 2024/2847 allows you to appoint an authorised representative in the EU by written mandate — but the mandate cannot cover design, development, production or vulnerability handling. Those remain yours. The representative holds your documentation and cooperates with authorities on your behalf.

The Cyber Resilience Act creates a specific framework for authorised representatives under Art. 18, distinct from the importer under Art. 19. An authorised representative is a natural or legal person established in the EU who has received a written mandate from the manufacturer (Art. 3(15)). Art. 18(3) defines the minimum mandate scope: retain the EU Declaration of Conformity and technical documentation for at least 10 years, provide documentation to authorities upon request, and cooperate with authorities on risk elimination. But Art. 18(2) sets a hard exclusion: the core manufacturer obligations under Art. 13(1)-(11) and Art. 13(14) — design, development, production, risk assessment, vulnerability handling, ENISA reporting — cannot be delegated. CRACheck generates the 8-document technical file your representative will hold. €149 per product. 15-25 minutes. Browser-side.

Generate CRA dossier — €149Free: check your product classification

€149 one-time · 8-document ZIP · 15–25 minutes · Browser-side

Built on Regulation (EU) 2024/2847 · Art. 31 + Annex VII · 8 PDF documents · 100% browser-side

Key figures

Art. 18
Defines the authorised representative mandate and its hard exclusions
10 years
Minimum documentation retention period by the representative (Art. 18(3)(a))
Art. 13(1)-(11)
Manufacturer obligations that cannot form part of the mandate

How to proceed

1
Confirm your manufacturer status under Art. 3(13)
You are the manufacturer if you develop or have developed a product with digital elements and market it under your name or trademark. If an EU entity places the product under its own brand, Art. 21 reclassifies that entity as manufacturer — and the representative structure does not apply to them.
2
Complete the technical documentation first
Art. 18(2) excludes Art. 13(1)-(11) from the mandate. You must complete the cybersecurity risk assessment, technical documentation, vulnerability handling setup and conformity assessment before the representative can hold anything.
3
Draft the written mandate
Art. 18(1) requires a written mandate specifying tasks. Art. 18(3) sets the minimum: retain declaration of conformity and technical documentation (Art. 18(3)(a)), provide documentation to authorities (Art. 18(3)(b)), cooperate with authorities on risk elimination (Art. 18(3)(c)).
4
Transfer the documentation package
The representative receives the 8-document technical file plus any engineering documentation per Annex VII. The representative must produce these within the timeframe authorities request.
5
Establish your ENISA reporting channel independently
Art. 14 reporting obligations remain with you. The representative does not submit notifications. Ensure your internal process meets the 24h/72h/14-day timelines from September 2026.
6
Maintain documentation throughout the support period
Art. 18(3)(a) requires retention for at least 10 years or for the support period, whichever is longer. Update the representative whenever documentation changes.

Common mistakes

MANDATE OVERREACH

Assuming the representative can handle ENISA notifications

Art. 18(2) of Regulation (EU) 2024/2847 explicitly excludes Art. 13(14) from the mandate scope. Art. 14 reporting — the 24h early warning, 72h notification, 14-day final report to ENISA — remains with the manufacturer. You cannot delegate vulnerability reporting to your EU representative.

ROLE CONFUSION

Conflating the authorised representative with the importer

Art. 3(15) defines the authorised representative as a mandated agent of the manufacturer. Art. 3(16) defines the importer as an EU person placing a product bearing a non-EU name. These are distinct roles. An importer has independent verification obligations under Art. 19. A representative acts within the manufacturer's mandate under Art. 18. One entity can serve as both, but the obligations stack — they do not merge.

DOCUMENTATION GAP

Appointing a representative before completing the technical file

The representative's core function under Art. 18(3)(a) is holding the declaration of conformity and technical documentation. If you appoint a representative before completing Art. 31 documentation, the representative has nothing to hold — and your product lacks the documentation Art. 31 requires at market placement.

What the ZIP contains

8 PDF documents generated from your data. Each cites the specific article of Regulation (EU) 2024/2847 it complies with.

1

Product Classifier

Identifies the CRA category. Your representative needs to know the classification to understand which conformity assessment route was followed.

2

Technical Documentation

The core Art. 31 and Annex VII document. This is what your representative holds under Art. 18(3)(a).

3

Risk Assessment

Cybersecurity risk assessment per Art. 13(2)-(3). Completed by you — the representative holds the result but does not produce it.

4

User Information

Annex II information and instructions. Your representative must produce this upon authority request.

5

Declaration of Conformity

EU Declaration per Art. 28 and Annex V. Art. 18(3)(a) specifically names this as a retention document.

6

CVD Policy

Coordinated vulnerability disclosure policy per Annex I Part II. Completed by you. Held by the representative.

7

Notification Template

ENISA notification template per Art. 14. You use this directly — the representative holds a copy for reference.

8

Obligations Calendar

Key CRA dates with representative retention obligations: 10-year minimum, support period milestones, ENISA reporting from September 2026.

See before you buy — Download sample dossier (PDF, fictional company) — Real structure, real articles, real format. Fictional data.

Generated from your data, in your browser. No data leaves your device.

What you pay

🧾 EU COMPLIANCE SERVICE PROVIDER — TYPICAL PACKAGE
Representative + documentation bundled
€3,000-8,000 per year per product family
Annual recurring contract
Documentation locked to provider's format
Switch cost if you change provider
Provider holds documentation, not you
✓ CRACHECK — DOCUMENTATION YOU OWN
8-document technical file, portable to any representative
€149 per product
15-25 minutes
Documentation belongs to you — transfer to any representative
Not locked to any provider
100% browser-side
30-day edit window, 10 regenerations
Permanent PDF

Two layers

● LAYER 1 — DOCUMENTATION · CRACHECK

The documentation layer — what CRACheck generates

CRACheck produces the structured technical documentation under Art. 31 and Annex VII that your authorised representative holds on your behalf. Eight PDF documents. One licence per product. The output is portable: transfer it to any representative in any EU member state. The documentation belongs to you, not to a service provider.

∅ LAYER 2 — NOT INCLUDED

What CRACheck does not do

CRACheck does not appoint an authorised representative. It does not draft the written mandate under Art. 18(1). It does not perform conformity assessment under Art. 32. It does not submit ENISA notifications under Art. 14. It does not act as your representative. CRACheck generates the documentation — the representative relationship is a separate commercial arrangement.

You produce the documentation. You appoint the representative. The representative holds what you produced. CRACheck handles the first step.

Enforcement regime

📅
11 September 2026 — Art. 14 reporting begins

ENISA reporting is your obligation as manufacturer. Your representative does not submit notifications. The 24h/72h/14-day process must be operational by this date regardless of your representative arrangement.

⚖️
11 December 2027 — Full CRA enforcement

Your product must carry CE marking, be accompanied by Annex VII documentation, and your representative must hold all documentation per Art. 18(3)(a).

🔒
Art. 64(3) — Up to €10,000,000 or 2% of global turnover

For non-compliance with Art. 18. Note: the manufacturer's own non-compliance with Art. 13 and Art. 14 falls under Art. 64(2) — €15M or 2.5%.

Alternatives

CriterioBundled representative serviceIn-house EU subsidiaryNo representativeCRACheck + separate representative
Documentation costIncluded (opaque pricing)Staff timeN/A€149 per product
Documentation ownershipProvider holds itYou hold itN/AYou hold it
Provider lock-inHigh — documentation tied to contractNoneN/ANone — portable PDF
Switching costRe-document everythingN/AN/AZero — transfer the PDF
CRACheck€149You own itNonePortable PDF

Multiple product lines entering the EU? Structure the documentation for all of them.

Pack 10: €99 per product. Pack 30: €79 per product. For non-EU manufacturers with large EU-bound catalogues, contact us for enterprise pricing.

Request volume pricing
Commercial enquiries via hello@solidwaretools.com

What CRACheck guarantees and what it does not

CRACheck generates a structured document set according to Art. 31 and Annex VII of Regulation (EU) 2024/2847 based on the information you provide. The accuracy of that information is your responsibility as manufacturer under Art. 13(1).

We guarantee that the document structure follows Art. 31 and Annex VII and that the legal references cited are correct. We do not guarantee acceptance by a specific market surveillance authority or that the documentation will satisfy a specific representative provider's internal requirements.

CRACheck is not legal advice. For questions about representative mandate scope, contractual structuring, or the interaction between Art. 18 and Art. 19, consult a qualified EU regulatory lawyer.

Frequently asked questions

Can a single entity serve as both authorised representative and importer?
Yes. Art. 3(15) and Art. 3(16) of Regulation (EU) 2024/2847 define distinct roles, but nothing prevents a single EU-established entity from holding both. However, the obligations stack: the entity would have the mandate duties under Art. 18 and the independent verification obligations under Art. 19. The documentation CRACheck generates serves both roles.
Does the authorised representative need technical expertise?
Art. 18(3) requires the representative to provide documentation to authorities and cooperate on risk elimination measures. This implies sufficient understanding of the documentation to respond to authority inquiries. The representative does not need to reproduce the technical file — only to hold it and make it available.
What if I change my authorised representative?
The documentation belongs to you as manufacturer. Transfer the CRACheck-generated PDF set to your new representative. The new representative assumes the Art. 18(3)(a) retention obligation from the date of the new mandate. Ensure continuity — there must be no gap during which no representative holds the documentation.
Does the CRA require all non-EU manufacturers to appoint an authorised representative?
Art. 18 uses permissive language: the manufacturer "may" appoint a representative. It is not mandatory. However, without a representative, you must fulfil Art. 18(3)-equivalent obligations yourself — including making documentation available to EU market surveillance authorities upon request. For practical purposes, most non-EU manufacturers appointing an importer under Art. 19 achieve equivalent market access without a separate representative.
Is this a subscription?
No. One-time payment. The licence includes 30 days of editing and 10 regenerations. The downloaded PDF is yours permanently.
Can I request a refund?
Under Art. 16(m) of Directive (EU) 2011/83, activating the licence constitutes express consent for immediate generation of digital content, waiving the 14-day withdrawal right. Refunds are only processed for reproducible technical failures.
What if the regulation changes?
If Regulation (EU) 2024/2847 is amended during your licence window, you can regenerate the documentation using the updated version of the generator at no additional cost.
⚠️ Important notice: CRACheck is a self-assessment documentation tool, not legal advice and not a third-party audit. The document under Article 31 and Annex VII of Regulation (EU) 2024/2847 is generated from your input data. You are responsible for the accuracy of the data you provide. CRACheck does not replace a qualified professional assessment.

Your documentation. Your representative. Your control.

Generate the 8-document technical file under Art. 31 and Annex VII. Transfer it to any authorised representative in the EU. €149 per product. Browser-side. No provider lock-in.

€149 one-time
8-document ZIP · 15-25 min · Art. 31 + Annex VII · 100% browser-side · Permanent PDF, 30-day edit window
Generate Technical Documentation
✓ Last regulatory check: 1 May 2026 · No substantive changes detected · View history