Tag Archives: MDR

Certification of medical devices in the context of the Reduce, Reduction and Replace EU Directive

By | June 27, 2019

The certification of a medical device can require animal testing: norms and ethical, and economic reasons impose a careful understanding of the mandatory steps for ensuring safety and efficacy of new technologies In this context, the European Union Directive 2010/63 / EU on the protection of animals used for scientific purposes constitute a milestone, but… Read More »

UBORA workshop at University of Bologna

By | February 28, 2019

In the context of the activities for promoting the UBORA platform and importance of harmonization of medical device regulation, an UBORA workshop was held at University of Bologna, the oldest University in Europe, on February 26th. The workshop, hosted in the course Biomedical Engineering for Developing Countries, thanks to the invitation of professor Stefano Severi,… Read More »