What Will Be the Economic Impact of the New Medical Device Regulation? An Interrupted Time-Series Analysis of Foreign Trade Data.

OBJECTIVES

To date, the economic effects of medical device directives compared with the clinical and regulatory effects have not been sufficiently studied. We believe that the financial obligations and responsibilities imposed on the stakeholders by the legal regulations have a corresponding economic indicator in the medical device market.

METHODS

In this study, we selected 2 crucial legal regulations on medical devices in Turkey: the Medical Device Directive that has been harmonized from the European Union and the Medical Device Sales, Advertising, and Promotion Directive. The impacts of these regulations on foreign trade were investigated using interrupted time-series analysis. Turkey's monthly medical device export and import data from 2008 to 2019 were obtained under 56 6-digit custom codes.

RESULTS

The results show that the selected directives have significantly affected the foreign trade trend level, and they may be breakpoints in the Turkey's foreign trade trend curve. We also reported the significant differences between the Medical Device Directive and the European Union's new medical device regulation (MDR) (2017/745 MDR).

CONCLUSIONS

We concluded that the MDR, which has more strict requirements, will result in increased costs for economic operators in comparison with the current directive and would further increase the import of medical devices by the importing countries. To prevent this, Turkey should aim to have a manufacturer's position by improving their clinical trial capabilities and manufacturing infrastructures with innovation-based approaches.