Newsletter | June 2022.
As a company that has developed a solution based on Artificial Intelligence (AI) and neuroscience ans as manufacturer of Medical Devices (MD), myBrain Technologies has to stay up to date with regulations and standards in these fields. For this, we can rely on our quality team! ...
![[DOWNLOAD] Artificial Intelligence Act: What future for AI in Europe?](https://emmanuel-guerin.fr/dev-mybraintech/wp-content/uploads/2022/06/white-paper-artificial-intellifence-act.png)
[DOWNLOAD] Artificial Intelligence Act: What future for AI in Europe?
With the increasing evolution of computing, robotics, and new technologies, AI is now a major part of our daily life. On April 21, 2021, the European Commission published a proposed regulation on Artificial Intelligence (AI), the Artificial Intelligence Act, which aims to establish safe and harmonized rules for this innovative field.
myBrain Technologies’s eye on Medical Device Regulation.
In order to improve health safety and harmonize rules within the EU, the Medical Device Regulation has been profoundly revised, resulting in new regulatory requirements - effective from May 26, 2021. To understand the difficulties of its application by manufacturers and find solutions, we interviewed Sophie Colliot.
