Pat Baird, Philips
An AI Medical Device Global Status Update (ISO, IMDRF, Legislation)
Pat gives an update on the regulation of Medical Devices based on ISO, IMDRF and Legislation.
Pat likes to think of his job as “Policy Engineering” – understanding the unmet needs (and frustrations) of regulators and developers, and developing standards, whitepapers, and training to meet those needs. He co-chairs over 10 committees at AdvaMed, AAMI, MITA, Xavier, CTA, and others on topics such as agile software development, cloud services for a regulated environment, and multiple committees on artificial intelligence in healthcare.