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---
title: "Annex VI"
type: regulation
legal_status: in_force
source: "https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02024R1689-20260727"
source_retrieved: 2026-10-02
shortTitle: "Annex VI"
instrument_type: level1_regulation
authority: Commission
binding: true
binding_character: binding
mica_level2: false
legal_basis: "Regulation (EU) 2024/1689"
instrument: aiact
celex: "32024R1689"
regulation: AI Act
regulation-full: "Regulation (EU) 2024/1689"
annex: VI
status: in_force
object_id: eu.aiact.legal_text.annex.vi
text_version: "Consolidated version of 27 July 2026"
source_url: "https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02024R1689-20260727"
check_status: matched
verified: true
last_checked: 2026-10-26
---

*In force · Consolidated version of 27 July 2026 · Checked against EUR-Lex on 26 Oct 2026 · [Official source](https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:02024R1689-20260727)*

### Conformity assessment procedure based on internal control

<a id="p-1"></a>**1.** The conformity assessment procedure based on internal control is the conformity assessment procedure based on points 2, 3 and 4.

<a id="p-2"></a>**2.** The provider verifies that the established quality management system is in compliance with the requirements of Article 17.

<a id="p-3"></a>**3.** The provider examines the information contained in the technical documentation in order to assess the compliance of the AI system with the relevant essential requirements set out in Chapter III, Section 2.

<a id="p-4"></a>**4.** The provider also verifies that the design and development process of the AI system and its post-market monitoring as referred to in Article 72 is consistent with the technical documentation.
