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Notified Body

A Notified Body is an independent third-party organisation accredited by an EU member state to conduct conformity assessments on behalf of manufacturers. Under the Cyber Resilience Act, Notified Bodies are required for Class II and certain Class I products that cannot self-certify compliance.

A Notified Body is an independent third-party organisation accredited by an EU member state to conduct conformity assessments on behalf of manufacturers. Under the Cyber Resilience Act, Notified Bodies are required for Class II and certain Class I products that cannot self-certify compliance.

CRA Regulatory

What Is a Notified Body?

A Notified Body is an independent conformity assessment organisation that has been formally accredited by a national accreditation body and notified to the European Commission by its member state. These organisations are authorised to perform third-party conformity assessments under specific EU legislation, issuing certificates that manufacturers need to affix the CE mark to their products. Under the Cyber Resilience Act, Notified Bodies carry out cybersecurity-focused assessments, examining whether a product's design, development processes, and vulnerability handling mechanisms meet the essential requirements set out in Annex I. A list of all notified bodies is published in the NANDO (New Approach Notified and Designated Organisations) database maintained by the European Commission.

CRA reference:Article 47

When Is a Notified Body Required Under the CRA?

The CRA establishes three conformity assessment routes. Default-class products (the vast majority) may self-certify via internal production control. Important Class I products have the option of using a Notified Body but may alternatively apply a harmonised standard and self-declare. Important Class II products - a smaller set of higher-risk categories such as hypervisors, industrial control systems, and smart meters - must involve a Notified Body unless they fully comply with a harmonised standard, in which case the manufacturer may self-certify using that standard's conformity route. Manufacturers of Class II products should begin engaging a Notified Body early in the product development lifecycle, as assessment timelines can extend to several months.

CRA reference:Article 32, Article 33

What Does a Notified Body Assessment Cover?

A Notified Body assessment for CRA purposes typically covers three areas. First, a review of technical documentation - verifying that security requirements have been identified, risk assessments conducted, threat models produced, and secure development processes followed. Second, an examination of vulnerability handling procedures - confirming that the manufacturer has a published CVD policy, a PSIRT function, a process for CVSS scoring and triage, and a mechanism for issuing security advisories. Third, testing of the product itself, either through review of existing test evidence or through independent testing, to verify that the essential cybersecurity requirements of Annex I are met. Notified Bodies issue EU-type examination certificates that are valid for a defined period and must be renewed when significant product changes occur.

CRA reference:Annex VII, Article 47

Choosing and Working With a Notified Body

Manufacturers should select a Notified Body with specific expertise in their product category - cybersecurity competence varies significantly between organisations. Key considerations include: whether the body is listed in NANDO for the relevant EU directive and CRA modules; the body's experience with software-intensive products; its capacity to assess vulnerability handling processes and not just hardware; and its geographic availability. Manufacturers should engage a Notified Body well before the CRA's compliance deadline for their product class. Providing complete technical documentation upfront, including threat models, SBOM, and vulnerability handling logs, significantly reduces assessment time and cost. CVD Portal's compliance export features are designed to generate the documentation artefacts Notified Bodies commonly request.

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Public CVD submission portal, acknowledgment tracking, Article 14 deadline alerts, and CSAF advisory generation. Receiving and tracking reports is free for all manufacturers placing products with digital elements on the EU market. Article 14 filing with the SRP-ready package is on Pro.

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Frequently asked

How do I find an accredited Notified Body for CRA assessments?+

The European Commission's NANDO database (ec.europa.eu/growth/tools-databases/nando) lists all notified bodies by directive and module. Once the CRA is fully operative, bodies notified specifically for CRA conformity assessment will appear there. Until then, manufacturers of higher-risk products should engage bodies already experienced in cybersecurity product assessment under RED or NIS2-adjacent frameworks, as these are most likely to gain CRA notification.

Can a manufacturer switch Notified Body mid-assessment?+

Yes, a manufacturer can change their Notified Body, but doing so will typically require restarting the assessment process, as each body conducts its own independent review. There is no automatic transfer of assessment work between bodies. Manufacturers should avoid switching unless there is a compelling reason, as it creates delays and additional cost.

How long is a Notified Body certificate valid?+

CRA EU-type examination certificates do not have a fixed universal validity period - this is set by the Notified Body and is typically three to five years. Certificates must be renewed when significant product changes occur that could affect compliance. The Notified Body may require re-assessment of specific areas when a product receives major security-relevant updates.

Related terms

Conformity AssessmentConformity assessment is the process by which a manufacturer demonstrates that its product meets the CRA's essential cybersecurity requirements. The process required depends on the product's classification: Default and Class I products can self-assess; Class II and Critical products require third-party assessment by a notified body.Conformity Assessment ProcedureA Conformity Assessment Procedure is the formal process by which a manufacturer demonstrates that a product meets applicable EU essential requirements before affixing the CE mark and placing it on the market. Under the Cyber Resilience Act, the required procedure depends on the product's risk classification.CE Marking (Cybersecurity)The CE mark is the mandatory conformity marking that manufacturers must affix to products with digital elements before placing them on the EU market under the CRA. It indicates that the product meets the CRA's essential cybersecurity requirements and has passed the applicable conformity assessment procedure.EU Declaration of Conformity (DoC)The EU Declaration of Conformity is a formal document signed by the manufacturer (or authorised representative) declaring that a product meets the essential requirements of all applicable EU regulations, including the CRA. It must be drawn up before the CE mark is affixed and kept available for market surveillance authorities for at least 10 years.Annex I Essential RequirementsAnnex I of the EU Cyber Resilience Act sets out the mandatory cybersecurity requirements that all products with digital elements must meet. It is divided into two parts: Part I covers secure product properties, and Part II covers manufacturer vulnerability handling obligations.Important Product Class IIImportant Product Class II is the highest risk tier under the EU Cyber Resilience Act's product classification system, covering products with digital elements whose compromise could have severe or widespread impact. Class II products - including industrial control systems, medical devices, and critical infrastructure components - face mandatory third-party conformity assessment.

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