Meet Our Regulatory Experts

Pathway Medical Device Advisors International offers unparalleled expertise in EU MDR regulatory consulting. Our team of experts brings decades of hands-on experience in the medical device industry, with a proven track record in designing, developing, and launching medical devices successfully.

What sets us apart is our deep understanding of the EU MDR process, honed through years of working at Tier-1 EU Notified Bodies. Our experts have not only worked with start-ups in high-pressure environments but have also driven regulatory excellence in Fortune 500 companies. Having been Notified-Body trained and certified in EU Regulatory Conformity Assessments for the EU, our experts know exactly what it takes to achieve compliance and get results fast.

At Pathway, integrity, work experience, and an unwavering work ethic are at the core of everything we do. Our commitment to your success ensures that we will navigate the EU MDR process efficiently, securing the outcomes you need. Let us put our expertise to work for you. We offer a 30 minute complimentary advisory consultation.