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AI Act Starter Kit

The essential quick guide to the EU AI Act

An overview of the new regulation and its demanding, imminent tasks for manufacturers of AI-based medical and IVD medical devices

 

Do you have the daunting task of studying the 140-plus pages of the EU AI Act, deriving its requirements, and implementing them accordingly?

Save yourself research and tedious work with our free AI Act Starter Kit. It provides an over­view of the new regulation and its demanding, imminent tasks. 

Gain Clarity

Get a compact overview of the EU AI Act's regulatory requirements and quick answers
​​​​​​​to the most important questions.

Efficient Planning

Find out what the EU AI Act specifically requires of you as medical device/IVD manufacturer and what tasks you need to complete.

Legal Certainty

Avoid costly redos and legal problems by imple­menting the legal requirements correctly and on time.

The free AI Act Starter Kit includes:

  • Mindmap of the chapter structure of the EU AI Act as a PDF and in XMind format 
  • List of links to further information and relevant legal texts 
  • FAQ on the EU AI Act with the most impor­tant and frequently asked questions 

Request your free AI Act Starter Kit

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