Dr. Schwabe, what problems are being addressed by the project?
Dr. Daniel Schwabe: More and more medical technology products that use AI algorithms are coming onto the market, and these products need to be certified. There is currently the Medical Device Regulation (MDR), and now the AI Act is being incorporated into the regulatory system. Some manufacturers are already overwhelmed, and it should never be the case that regulation slows down innovation.
The EU project TEF-Health (Testing and Experimentation Facility), which is funded with 60 million euros, is designed to certify AI medical devices in the future. The Metric Framework is our first step towards supporting these processes by providing a systematic way of checking training and test data. To increase the trustworthiness and safety of AI medical products, such validation will be necessary in the future.
What is the status quo regarding data quality in medical AI applications?
Schwabe: There is a broad spectrum. We are not trying to evaluate general data for all applications, but want to know: How can we systematically analyze whether this data set that I have available fits the application that I am currently developing? We try to take a very practical approach to the question, always with a view to the manufacturers, especially SMEs and start-ups. They develop innovations, but often do not yet have the necessary infrastructure and knowledge in terms of quality assurance. We want to provide them with a system that they can use to evaluate their data.