One of the objectives of the iToBoS project is to acquire a large dataset with different types of lesions from patients with diverse skin types, different phenotypes, and different degrees of UV damage.
This article summarizes the main differences between MDR and the previous MDD; the first one is the new rules have the legal form of “regulation” and in contrast to “directive”, it enters directly into force in the EU Member States and does not have to be transferred into national law.
Despite the technology risks related to AI, the MDR regulatory frameworks does not include any specific requirements for the use of artificial intelligence in medical devices and no law, common specifications or harmonized standards exist to regulate AI application in medical devices.
In the MDR there is no special change for embedded software products; they follow the classification of the device of which they are a part.
An overview of the new European Regulation on medical devices (MDR).
AI is rapidly transforming medicine and health care, allowing for significant advancements in fields such as medical diagnostics, drug development, treatment personalization, supportive health services, genomics, and public health management.