After the four-year transition period: Is the European Union's Medical Device Regulation of 2017 likely to achieve its main goals?

Following a series of major scandals over the past two decades, the medical device industry is now undergoing a major regulatory change: the implementation of the European Union Medical Device Regulation (MDR) of 2017. After a transitional period of four years, the MDR became fully binding in May 2021. Although the medium- and long-term impacts of the MDR are still unclear, a range of scholars, health care professionals, and industry representatives have begun to publish early evidence and publicize their views on how the new regulation may impact free trade and patient safety. Even a cursory view of their output reveals hypotheses and opinions that could hardly be more divergent. The reasons for this disagreement are unclear and may extend beyond the different interests of the various stakeholder groups. To find out why this might be the case, we examine the MDR and seek to improve scholarly understanding of this most extensive regulation of medical devices since the early 1990s. We offer policymakers suggestions to help them improve future regulation. Based on theoretical considerations, we conclude that while the MDR is highly likely to strengthen the internal market of the EU, its impact on patient safety will remain unclear as long as there are no comprehensive studies on this topic that are based on empirical data.

Automated summary

The implementation of the European Union Medical Device Regulation (MDR) has brought significant regulatory changes to the medical device industry. While the medium- and long-term impacts of the MDR are still uncertain, there is a divergence of opinions regarding its effects on free trade and patient safety. Through an analysis of the MDR, it is suggested that it is likely to strengthen the EU internal market, but its impact on patient safety remains unclear without comprehensive studies based on empirical data.