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Who Issues Documents Under CE AVCP Systems?
There is no single issuer of every AVCP output.
Continue with the relevant decision step
Direct answer
There is no single issuer of every AVCP output. Depending on the applicable system, the third-party output may be a product certificate, an FPC certificate or a laboratory report. The manufacturer remains responsible for its performance declaration and CE marking.
Decision and evidence
Verify the organisation's current product, reference and task designation. Distinguish a technical assessment body preparing an ETA from a body performing the required AVCP task.
Technical basis
For construction products, the harmonised specification or ETA and intended use determine AVCP 1+, 1, 2+, 3 or 4. The number is a division of tasks, not a quality grade.
Related practical guide
Construction Product AVCP: Duties, Documents and Technical Transitions
Primary sources and currency
This page was technically reviewed on 22 August 2026 against the primary sources below. The current legislation, standard edition and official fee schedule at the application date take precedence.
European Commission — CE marking for manufacturers ↗European Commission — Conformity assessment ↗European Commission — NANDO notified bodies system ↗EOTA — European Technical Assessment (ETA) ↗Practical questions
Can a numbered notified body assess every construction product?
Verify current product, specification and task scope in official records. Designation in another area is insufficient. Testing, product certification and FPC certification can be separate functions. Matching the required output to the correct scope before application reduces wasted time and cost.
Does an FPC certificate under System 2+ end the manufacturer's testing duties?
Identify manufacturer and notified body tasks separately from the applicable framework. FPC certification does not replace product assessment or control records. Specify who tests what and how often. Surveillance does not transfer every daily production decision to the body.
Let us define the correct scope together.
Share the product or activity, site, target market, existing evidence and target date. Kayra Patent will explain a practical preparation and coordination route.