ConformanceHouse
Getting started · Updated 14 September 2026

What to do about the CRA, in order

Short answer. Three things decide the shape of everything else. Do them first, in this order.

  1. Does it apply? Ten minutes. If the answer is no, stop.
  2. Which class? This decides whether you sign your own declaration or wait for a notified body. It is the only answer that can add months.
  3. How long will you support it? One number that drives the retention duties, the user information and part of the technical file.

Then: the reporting process this week, because that duty is already live. Then the documents, which are due 11 December 2027.

Search for a CRA checklist and you will find flat lists of twenty-five or thirty items, which implies they all matter equally and can be tackled in any order. They cannot. Some items have dependencies on other people's calendars; some are already overdue; most are not due for more than a year. Getting the order right is worth more than getting the list complete.

The three decisions that come first

1. Does the regulation apply to this product?

Three tests, and each one is capable of ending the enquiry: is it placed on the EU market; is it a product rather than a service; and is it supplied in the course of a commercial activity. A pure cloud service is generally out. Unmonetised open source is out. Medical devices, vehicles, aircraft and marine equipment are out because other regimes cover them. The full scope rules, or the two-minute check.

2. Which class is it?

Look your product up against Annex III and Annex IV. Most products are on neither list, which means the default category and self-assessment: no notified body, no external audit, no certification fee, and a timeline you control. If you are on one of those lists the answer changes materially, and for Class II and Annex IV a third party is now in your critical path. How the two lists work.

Do this second, and do it properly. It is the only decision in the whole exercise that can add months rather than days, and the only one where being wrong is expensive rather than correctable.

3. How long will you provide security updates?

The support period must reflect how long the product is expected to be in use, and must be at least five years unless it is expected to be in use for less. Pick the number deliberately, because it propagates:

What a long support period actually commits you to.

This week: the duty that is already live

The reporting obligations in Article 14 have applied since 11 September 2026. Everything else is future work. This is not.

What "being ready" actually means, and none of it takes long:

  1. Create the EU Login account for whoever will file, with two-factor enabled, and register on the ENISA single reporting platform. Reports are filed manually, and an account cannot be created inside a 24-hour window.
  2. Work out which CSIRT you report to. It follows from where your cybersecurity decisions are predominantly taken, not from where the company is registered. The routing rule, and the trap in it.
  3. Name the person who files, and their backup. Write both names down somewhere the on-call person can find them.
  4. Pre-draft the reports. Your company details and product identifiers do not change during an incident; fill them in now so the 24-hour window is spent on the incident.
  5. Know the four deadlines, and in particular that neither final-report clock starts at discovery. The two tracks, and the clocks people get wrong.
One genuine piece of relief, if you are small. Article 64(10)(a) disapplies administrative fines for manufacturers that qualify as microenterprises or small enterprises in respect of any failure to meet the 24-hour early-warning deadline. It covers that deadline only, it removes the fine rather than the duty, and "small enterprise" is a defined term that counts linked and partner enterprises. But it is real, and it is aimed at the hardest deadline in the regulation. The penalty tiers, and the exemption in full.

This quarter: the things with lead times

Everything in this section depends on somebody else, which is why it goes before the writing.

TaskWhy it cannot wait
If you need a notified body, start finding one The bodies are newly designated, demand will not be evenly spread across the months before December 2027, and the procedure has to finish before you can place the product on the market
Appoint an authorised representative if you are outside the EU A mandate has to be agreed and documented, and the representative's details go on the declaration of conformity
Decide where your documents will live for ten years If you cite an internet address in your user information, that address has to resolve for a decade. Choosing it after you have printed it is too late
Write the vulnerability disclosure policy and publish it It is required by Annex I Part II, it has to be findable by users, and it is the one document that costs nothing but an afternoon
Set up the reporting inbox and make sure a human watches it The single point of contact has to work, and it has to still work when the person who set it up has left

Before December 2027: the documents

The substantive obligations apply from 11 December 2027. That is not a grace period in any useful sense — the technical file has to describe a product that was designed to meet Annex I, which is not something you can assemble retrospectively — but it is the date the paperwork is measured against.

Five documents, and the order below is the order that avoids doing work twice:

  1. The cybersecurity risk assessment first. It addresses each of the thirteen requirements in Annex I Part I, and its answers feed everything else. With the harmonised standards still in development there is no standard to cite instead, so this document carries more weight in your file than it would under a mature regime.
  2. The user information, because seven of its nine points are facts you have already written down. The nine points.
  3. The support period justification, which is one or two paragraphs recording the reasoning behind decision three above.
  4. The technical documentation, which is largely an index to the other documents plus the architecture description and the test reports. Annex VII, point by point.
  5. The declaration of conformity last, because it is the claim the other four support. What signing it commits you to.

Alongside them: generate an SBOM per release from your existing build tooling, and store it with the version of the product it describes. The statutory floor is the top-level dependencies, so this is a command rather than a project. What the CRA actually asks for.

Forever: the duties that recur

The mistake in treating this as a project is that half of it is not one. Annex I Part II is a process, and Article 13 is a filing obligation with a ten-year memory.

What can safely wait

Worth saying explicitly, because a flat checklist implies otherwise:

Why this order, and not a different one

Three dependencies drive it, and they are the reason a flat list produces wasted work:

Classification gates the documentation. Writing a technical file before you know whether a notified body has to examine it risks writing the wrong file, and — more importantly — discovering the lead time late.

The support period propagates. It appears in the user information, at the point of purchase, in the technical documentation and in the retention dates. Changing it after those are written means changing all of them.

Reporting is live and everything else is not. A process you can execute inside 24 hours is worth more this month than a document that is not due for fourteen. It is also the cheaper of the two to get ready.

How to check everything on this page. The application dates are in Article 71 of Regulation (EU) 2024/2847; the reporting duties in Article 14; the manufacturer's obligations and the retention duties in Article 13; the essential requirements in Annex I; the conformity assessment routes in Article 32; the classification lists in Annexes III and IV; and the document contents in Annexes II, V and VII.

An honest note on confidence: this page is a sequencing opinion built on the material in the linked guides, and each of those states its own confidence. The two application dates are corroborated across several independent sources. The claim that the harmonised standards are incomplete and have slipped comes from the standards bodies' own published schedules and can move again. Nothing here is legal advice, and the order that suits your product may differ — particularly if you already CE-mark under another regime, in which case your existing conformity process is the right place to start rather than a blank page.

Steps 1 and 2, in two minutes

The free check works through the scope tests and the classification lists and tells you which category you are in, whether you can self-assess, and which documents you have to produce.

Take the free check

Then, if the documents are the work: Conformance House produces them from one questionnaire and keeps every dated version for the ten years the regulation asks for — €390 a year for one product.