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.
The new European Regulation on medical devices (MDR).
While the GDPR provides a strong legislative foundation to protect the rights and freedoms of European individuals, it cannot (and does not) govern all aspects that influence the direction of the iToBoS project.
An article about the the conundrum of health data in a world of AI-enhanced diagnosis in iToBoS project.
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.
One of the key challenges of research in the field of computer science is assembling the appropriate infrastructure needed for scientists to successfully carry out their work.
Today, we spoke to Marjolein van Kessel from Naevusglobal.
Today, we spoke to Karen Gorp, one of our colleagues from Melanoma Patients Australia about why she thinks Early Detection is important for Melanoma patients and her hopes for iToBoS!