Venture Challenge alumnus Prolira received EU MDR certification

23 Jun 2020. Prolira is one of the first medical device companies in the world to be certified according to the new EU MDR. The European Medical Device Regulation (EU MDR) guarantees safety and quality requirements for medical devices being manufactured or imported Ito Europe. it underwent fundamental revisions in 2017 to improve transparency through standard data, technological advances and the creation of an EU (EUDAMED) database. While the MDD was simply a set of guidelines, MDR is legally enforceable by EU member states. Source: Prolira