AI Chatbots & Assistants

Three pillars for trustworthy AI development

How can we build trusted solutions with such a young technology such as AI?

Transparency

A system’s decision making needs to be transparent with respect to performance metrics and the data used to train the system.

Process

A trustworthy system needs to be developed with a thorough and systematic process based on established best practices.

Certification

Prepare your AI for regulation

AI systems are decision-making systems. To realize the full potential of AI trust in those decisions is key. This is especially true if your AI is used in a mission-critical area, such as finance, logistics, or R&D, or in a safety-critical domain, such as medical devices or driver assistance. The EU AI Act regulates the use of AI in a wide range of high-risk areas, including infrastructure, employment, essential financial services, education, and others. AI in critical areas needs to be safe, robust, and fair.

Benefit from our experience

We are member of the KI Bundesverband, an alliance of 400+ AI companies dedicated to ethical AI.

We have gained the TRUSTIFAI certificate by TÜV Austria for a medical imaging application.

Is my system high-risk under the EU AI Act?

EU Regulated Domains

Any AI system that falls under one of the following categories is high-risk, and has to be registered in the EU database:

Biometric identification
Operation of critical infrastructure
Access to education
Access to and management of employment
Access to essential public/private services (for example insurance, credit)
Law enforcement
Migration, asylum and border control

Generative AI

GenAI must comply with transparency requirements, disclose that the content was generated by AI, and where to find summaries of copyrighted data used for training. Also, the model must be designed such that generating illegal content is prevented.

EU Product Safety Legislation

An AI System used in products falling under the EU's product safety legislation, including toys, aviation, cars, medical devices or lifts, will be considered high-risk, and will therefore be regulated.