More and more medical devices use artificial intelligence (AI) and machine learning (ML) to perform or support medical applications. Despite the risks involved, these new technologies are not sufficiently considered in the current legal framework for medical devices (e.g. MDR, IVDR). In this webinar we want to present key features of AI in the medical field, considering the huge benefit as well as the risk associated with application of AI. Furthermore, the current global AI regulation framework is outlined in addition to what a medical device manufacturer needs to consider before placing a medical AI into the markets. The three main topics discussed:
This webinar does not expect high technical background and is aimed at developers, managers, regulators and regulatory affairs personal to understand the current status of AI in the medical field.
Fill out the form to learn the key features of AI in the medical field as well as the current global AI regulation framework.
Dr. Abtin Rad
Global Director Functional Safety, Software and Digitization, TÜV SÜD
Dr. Abtin Rad has 13 years of professional experience as a Biomedical and electrical Engineer with focus on Software, Cybersecurity and Artificial Intelligence, as well as medical Imaging and Therapy using Ultrasound and optical laser systems. Dr. Abtin Rad is a Cybersecurity and Artificial Intelligence Specialist for medical devices and medical software, as well as a Lead Auditor for ISO 13485, ISO 9001, MDSAP and MDD/MDR.
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Bosnia and Herzegovina