The EU AI Act is a landmark legislation that will shape the future of AI in Europe and is expected to be the baseline for ...

The deadline for medical devices compliance to the new medical devices regulation 2017/745 (EU MDR) was originally May 2020 for class l non-sterile devices and May 2024 for all other devices. During ...

Bovine collagen has long been valued as a biomaterial in medical devices due to its biocompatibility, scaffold properties for cell growth, and hemostatic qualities. Despite widespread global use, ...