As the implementation deadlines quickly approach, many medical device companies have not adequately prepared for the new EU Medical Device Regulation (MDR). In addition, how much will compliance with the regulation cost? With the help of industry expertise, MedTech Intelligence has developed a survey to gauge industry’s estimate on costs of the entire compliance effort related to the EU MDR. We invite you to take the survey, the results of which will be revealed in the weeks leading up to the MedTech Intelligence EU MDR Implementation Strategies Workshop, November 27–28 in Washington, D.C. (you can also attend virtually).
You can adjust all of your cookie settings by navigating the tabs on the left hand side.