11.09.2024 // Position Paper
MDR and IVDR: End regulatory overload, maintain high protection level
... Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR) came into force on 26 May 2017 and replaced the three directives (MDD, ...
#ai#eu single market#medical products
20.07.2023 // Position Paper
Recommendations for the AI Act trilogue negotiations
... With the Artificial Intelligence Act (AI Act), the European Union aims to become a pioneer in the regulation of AI. The aim is to enable the trustworthy and safe use of AI systems and to ensure the ...
#position#ai
16.08.2021 // Position Paper
Statement on the proposal for an Artificial Intelligence Act by the European Commission
... A robust regulatory framework is a fundamental prerequisite for building the necessary trust in AI-based products and systems and, with it, the acceptance of this new digital technology. The TÜV ...
#position#ai#digitalization
25.03.2019 // Position Paper
Create trust in AI-based systems and products
... Although artificial intelligence (AI) is not a new phenomenon from a scientific point of view, political interest in the issue has grown significantly in recent years. Due to the increasing use of ...
#position#european elections#ai#digitalization