EU AI Act — High-Risk Systems

Categories: EU AI Act

About Course

EU AI Act — High-Risk Systems is the practitioner-depth companion to EU AI Act Foundations, taking you inside the substantive Chapter III obligations that fall on providers and deployers of high-risk AI systems.

Structure

10 modules covering each Chapter III obligation.
40 CPD hours over 8-10 weeks.
One summative assessment — a three-artefact compliance package.

Establish whether a system is high-risk under Article 6 and Annex III.
Design a risk management system that meets Article 9.
Structure data governance to Article 10 standard.
Produce technical documentation to Annex IV.
Design meaningful human oversight per Article 14.
Prepare for conformity assessment under Annex VI.
Build post-market monitoring per Article 72.

Course Content

Module 1. Determining high-risk status

Lesson 1.1: The high-risk classification decision, in depth
Lesson 1.2: Working through Annex III systematically
Lesson 1.3: Common classification mistakes and how to avoid them
Module 1 Check

Module 2. The provider role and the value chain

Module 3. Quality management (Article 17)

Module 4. Risk management (Article 9), in depth

Module 5. Data and data governance (Article 10), in depth

Module 6. Technical documentation (Article 11, Annex IV)

Module 7. Human oversight (Article 14) and transparency (Article 13)

Module 8. Accuracy, robustness, cybersecurity (Article 15) and logging (Article 12)

Module 9. Conformity assessment (Article 43) and market entry

Module 10. Integrated compliance file — the capstone

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About Course

Structure

What Will You Learn?

Course Content

Module 1. Determining high-risk status

Lesson 1.1: The high-risk classification decision, in depth

Lesson 1.2: Working through Annex III systematically

Lesson 1.3: Common classification mistakes and how to avoid them

Module 1 Check

Module 2. The provider role and the value chain

Lesson 2.1: Who is the provider — and when does that change

Lesson 2.2: When a deployer becomes a provider

Lesson 2.3: Mapping obligations across the value chain

Module 2 Check

Module 3. Quality management (Article 17)

Lesson 3.1: The overarching QMS — Article 17 and its integrations

Lesson 3.2: Integrating Article 17’s QMS with existing systems

Lesson 3.3: Preparing the QMS for conformity assessment scrutiny

Module 3 Check

Module 4. Risk management (Article 9), in depth

Lesson 4.1: The Article 9 RMS at practitioner depth

Lesson 4.2: The Article 9 risk management system as a continuous process

Lesson 4.3: Testing requirements and their documentation

Module 4 Check

Module 5. Data and data governance (Article 10), in depth

Lesson 5.1: Article 10 as a working practice

Lesson 5.2: Data quality criteria under Article 10

Lesson 5.3: Data governance across the sourcing lifecycle

Module 5 Check

Module 6. Technical documentation (Article 11, Annex IV)

Lesson 6.1: Building the Annex IV documentation package

Lesson 6.2: Working through the Annex IV checklist

Lesson 6.3: Common technical documentation failures

Module 6 Check

Module 7. Human oversight (Article 14) and transparency (Article 13)

Lesson 7.1: Meaningful human oversight in practice

Lesson 7.2: Designing human oversight measures that satisfy Article 14

Lesson 7.3: Transparency and instructions for use under Article 13

Module 7 Check

Module 8. Accuracy, robustness, cybersecurity (Article 15) and logging (Article 12)

Lesson 8.1: Article 15 as an engineering-compliance interface

Lesson 8.2: Accuracy, robustness, and cybersecurity as ongoing obligations

Lesson 8.3: Article 12 logging requirements in practice

Module 8 Check

Module 9. Conformity assessment (Article 43) and market entry

Lesson 9.1: The conformity assessment gateway

Lesson 9.2: Choosing between self-assessment and notified body routes

Lesson 9.3: Registration, CE marking, and the EU database

Module 9 Check

Module 10. Integrated compliance file — the capstone

Lesson 10.1: Assembling the compliance file

Summative assessment brief

Lesson 10.2: Structuring the compliance file end to end

Lesson 10.3: Maintaining the compliance file after market entry

Module 10 Check

Student Ratings & Reviews