AI tools are being purchased and deployed in radiology departments across Europe. This webinar gives imaging professionals the vocabulary and criteria to participate meaningfully in procurement and adoption decisions, covering how to read a validation study critically, what questions to ask a vendor, what regulatory marks mean (CE, FDA clearance, MDR class), and what red flags to look for.

Biomarker research is one of the fastest-growing areas in radiology, but getting it right, reproducibility, standardisation, regulatory requirements, is far from straightforward. This session will provide a practical grounding in the essentials of biomarker research, the ESR EIBALL Biomarker Inventory and other frameworks and reproducibility requirements.

Following last year’s popular course, we are now offering an updated and expanded session on writing and publishing in an AI environment. Journal AI policies are evolving to keep up with the pace of technology and we now offer a fresh treatment covering the responsible use of writing tools, predatory journal identification, and the importance of peer review process.

This session follows up and expands on last year’s session on writing a PhD, offering more advice and insights that might help you decide if a PhD is for you.

During this webinar our speakers will translate the regulatory and legal landscape into practical, scenario-based guidance to help you understand medicolegal responsibility, liability, and the EU AI Act.

As part of a new ESR partnership with Euro-BioImaging, this session introduces members to a concrete research asset: open access to imaging technologies, analysis services, and FAIR data support across European nodes.