Training course – EU AI Act & AI Compliance – Healthcare

EU AI Act & AI Compliance for Healthcare Professionals

Putting the EU AI Act into practice: risk categories, deployer obligations, AI literacy under Art. 4, AI policy and GDPR interfaces.

Duration
6 hours, one session
Format
Online or on-site
Language
German or English
Participants
open dates or exclusive for your team
Certificate
Certificate of attendance

Overview

“EU AI Act & AI Compliance for Healthcare Professionals” is a hands-on course for roles such as Physicians in hospitals and practices, Nurses and nursing managers and Hospital and practice managers. Rather than learning EU AI Act & AI Compliance in the abstract, you work on tasks from your daily routine – with examples, exercises and templates from Healthcare.

The EU AI Act is the first comprehensive legal framework for artificial intelligence, and it applies not only to providers but also to organisations that use AI systems in their daily work. In this compact course you will learn how the regulation is structured: prohibited practices, high-risk systems, transparency obligations and general-purpose AI models. You will find out which role your organisation plays as a deployer, which obligations follow and how to record and classify the AI applications you use in a structured way.

The practical part turns the requirements into manageable steps. You clarify what the AI literacy obligation under Article 4 means in concrete terms, how to organise training in a verifiable way and what an internal AI policy should cover. You also examine the interfaces with the GDPR, such as legal bases, data protection impact assessments and automated decision-making. You leave with an AI inventory template, a draft policy and a clear compliance roadmap for your area of work.

Hospitals, practices, care homes and health insurers struggle with staff shortages and a heavy documentation burden that takes valuable time away from patients. Generative AI can provide targeted relief: AI assistants help draft discharge letters and reports, summarise guidelines and studies, write patient information in plain language and support quality reports, rosters and administrative tasks. Automation speeds up appointment management, enquiry handling and internal communication. At the same time, the strictest requirements apply: health data is specially protected, medical confidentiality and professional rules must be observed, and software with a medical purpose may qualify as a medical device. AI in healthcare must therefore distinguish clearly between administrative support and clinical decisions, be operated securely and remain under the responsibility of qualified professionals.

The course is delivered live – either online in a virtual classroom or on-site in our training rooms in Munich, Salzburg, Berlin, Augsburg, Hanover, Bremen, Stuttgart and Kaiserslautern. We can also run it exclusively for your team.

Who is this course for?

  • Physicians in hospitals and practices
  • Nurses and nursing managers
  • Hospital and practice managers
  • Clinical coding and medical controlling staff
  • Quality management and administration in healthcare facilities

Typical challenges we address

  • Coping with heavy documentation alongside patient care
  • Keeping up with current guidelines and evidence
  • Informing patients clearly and in several languages
  • Running administrative, quality and billing processes with limited staff

What you will be able to do

  • You can explain how the EU AI Act is structured and assign your organisation to the correct roles.
  • You can classify the AI applications in use by risk category and maintain an AI inventory.
  • You can name the specific obligations of deployers and derive appropriate measures.
  • You can develop an AI literacy concept under Article 4 and a draft internal AI policy.
  • Use AI to reduce the burden of documentation, patient information and administration.
  • Distinguish confidently between administrative AI applications and regulated medical devices.
  • Protect patient data in line with the GDPR, medical confidentiality and professional rules.

Course outline

Module 1 Structure and logic of the EU AI Act
  • Objectives, scope and phased application of the regulation
  • Roles at a glance: provider, deployer, importer and distributor
  • The risk-based approach: prohibited practices, high risk, limited risk and minimal risk
  • Specific rules for general-purpose AI models
Module 2 Classifying risk in practice
  • Prohibited practices such as social scoring or emotion recognition in the workplace
  • High-risk areas under Annex III, including recruitment, creditworthiness and education
  • Transparency obligations for chatbots, synthetic content and deepfakes
  • Recording and classifying your own AI applications in an AI inventory
Module 3 Obligations for deployers of AI systems
  • Use in line with instructions and human oversight by competent staff
  • Input data quality, monitoring of operation and retention of logs
  • Informing employees and affected persons and reporting serious incidents
  • Fundamental rights impact assessment: when it is required and how it works
Module 4 AI literacy under Art. 4 and internal AI policy
  • What sufficient AI literacy means for different roles
  • Designing training concepts and documenting measures verifiably
  • Components of an AI policy: approved tools, data classes, approvals and labelling
  • Responsibilities, AI officers and involving the works council and IT
Module 5 GDPR interfaces and governance
  • Legal bases, purpose limitation and data minimisation when using AI
  • Data protection impact assessment and its relationship to the fundamental rights assessment
  • Automated individual decisions, data subject rights and data processing agreements
  • Compliance roadmap: priorities, ownership and regular review
Module 6 Practice lab: Healthcare
  • Drafting letters and reports
  • Summarising guidelines and studies
  • Patient information
  • Nursing documentation support
  • Quality and administrative documents
  • Enquiry and appointment management
Module 7 Data protection, quality & transfer to daily work
  • Health data is a special category under Article 9 GDPR and subject to medical confidentiality, in Germany under Section 203 of the Criminal Code; it may only be processed in approved, contractually secured environments. Software with a medical purpose, such as diagnostic or therapy support, can be a medical device under the MDR and is then high-risk AI under the EU AI Act.
  • Ground rules for safe AI use in your team
  • Checking results: facts, sources, tests and the four-eyes principle
  • Personal action plan for the next 30 days
  • Open questions, outlook and resources for further learning

Practical scenarios from your field

Drafting letters and reports

An AI assistant in an approved environment structures findings and progress notes into a draft discharge letter or report, which the responsible physician fully reviews and corrects.

Summarising guidelines and studies

AI summarises guideline recommendations, studies and product information and compares key statements, as a starting point for continuing education and with references to the original sources for verification.

Patient information

Clinical content is turned into clear patient information, plain-language supplements to consent materials and leaflets in several languages, which are medically reviewed and approved.

Nursing documentation support

AI helps turn bullet points into structured nursing reports and handovers, draft care plans and harmonise wording, while the nurse remains responsible.

Quality and administrative documents

Procedures, hygiene plans, quality reports and training materials are created and updated with AI support, without the need for any patient data.

Enquiry and appointment management

Automations sort incoming enquiries from patients and referring physicians, answer standard organisational questions and prepare appointment suggestions, while medical questions go to qualified staff.

Prerequisites

No legal background is required. A basic knowledge of the GDPR and an overview of the AI applications used or planned in your area are helpful. You work in a healthcare organisation, in a clinical, nursing, administrative or management role.

Technical requirements

All you need is a laptop with an up-to-date browser and an office suite for working with templates. No special AI licences are necessary.

Data protection & compliance

Health data is a special category under Article 9 GDPR and subject to medical confidentiality, in Germany under Section 203 of the Criminal Code; it may only be processed in approved, contractually secured environments. Software with a medical purpose, such as diagnostic or therapy support, can be a medical device under the MDR and is then high-risk AI under the EU AI Act.

Dates & locations

For every location we suggest a date roughly four weeks ahead. Your preferred date is always possible.

  • Munich Mon, 14 December 2026 6 hrs Request
  • Salzburg Fri, 11 December 2026 6 hrs Request
  • Berlin Tue, 15 December 2026 6 hrs Request
  • Augsburg Tue, 15 December 2026 6 hrs Request
  • Hanover Mon, 14 December 2026 6 hrs Request
  • Bremen Fri, 11 December 2026 6 hrs Request
  • Stuttgart Thu, 10 December 2026 6 hrs Request
  • Kaiserslautern Mon, 14 December 2026 6 hrs Request
  • Online Wed, 16 December 2026 6 hrs Request

Frequently asked questions

Does the EU AI Act apply to companies that only use AI tools?

Yes. Anyone using AI systems under their own authority in a professional context is a deployer. All deployers must, in particular, ensure that their staff have sufficient AI literacy. Where high-risk systems are used, for example in recruitment, further obligations apply, such as human oversight, logging and informing the people affected.

Does this course satisfy the training obligation under Article 4?

The course covers core AI literacy content and you receive a certificate of attendance that you can add to your documentation. However, Article 4 requires measures tailored to role, prior knowledge and context of use. That is why you also learn how to set up and maintain your own AI literacy concept for your organisation.

Does the course replace legal advice?

No. The training provides practical knowledge for specialists and managers so they can interpret requirements, ask precise questions and implement first measures. For binding assessments of individual systems, especially in high-risk areas, you should involve your legal department, your data protection officer or external specialist lawyers.

May patient data be processed in AI tools?

Only in environments approved by your organisation, secured under data protection law and compatible with medical confidentiality. Publicly available consumer tools are unsuitable. Many use cases, such as quality documents or patient information, need no patient data at all. We show you how to get started safely.

When does AI software become a medical device?

The intended purpose is decisive: software intended for diagnosis, monitoring or therapy decisions for individual patients can fall under the MDR. General text and administrative support usually does not. In the course you learn to recognise this boundary and keep clinical decisions with qualified professionals.

How much does “EU AI Act & AI Compliance for Healthcare Professionals” cost?

The course costs a flat €949 plus VAT per participant – whether online or on-site. This includes 6 hours of live training with a trainer, course materials, a lab environment and a certificate of attendance.

Can I suggest my own date?

Yes. For every location we suggest a date roughly four weeks ahead. In the request form you can always describe your preferred date or period in free text – we check availability and get back to you within one working day.

Is the course online or on-site?

Both are possible: live online in a virtual classroom or on-site in Munich, Salzburg, Berlin, Augsburg, Hanover, Bremen, Stuttgart and Kaiserslautern. We can also run the course exclusively for your team.

Can the course be tailored to our team?

Yes. Tailor-made courses cost approx. €4,500 more, depending on the topic and by arrangement. We agree content, examples and exercises with you in advance.

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