The European Union Medical Device Regulation (EU MDR) (2017/745) was approved by the European Parliament on May 25, 2017. This new medical device change recognizes historical medical device problems and aims to strengthen regulatory requirements and oversight to foster a more FDA-like regulatory environment. The mandatory deadline for compliance is fast-approaching...don't miss it!
We are currently offering a Free 30 Minute Consultation to help you navigate EU MDR. To schedule your Free 30 Minute Consultation, just fill out the form, and one of our team members will be in touch to set up your meeting.
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Since 2012, Professional Resource Partners (PRP) has been honored to serve as a trusted source of quality and regulatory compliance consultants to the medical device and diagnostics industries. In 2017, we launched PRP Quality which specializes in Automotive Quality inspection, sorting, and containment. As an ISO:9001 Certified Business and a WBENC Certified Woman-Owned Business, our company is proud to deliver exceptional professional integrity and service to the many clients we support with our customized approach. It’s also the reason why, when PRP is involved, client expectations are not simply met, but they are consistently surpassed.
