At Quality Commercial Consultants, we help medical device companies navigate the complexities of regulatory compliance, quality management, and cybersecurity. With deep expertise in FDA 510(k) submissions, EU MDR, ISO 13485 QMS implementation, and medical device cybersecurity, we provide strategic guidance to ensure your products meet global standards while accelerating time to market.

Led by principal consultants Andy Miller, a seasoned consultant with decades of experience in medical device regulation, quality assurance, and cybersecurity compliance, our team partners with startups and established manufacturers to streamline compliance, reduce risk, and optimize processes. We combine technical expertise with a practical, results-driven approach to help you succeed in an evolving regulatory landscape.

Whether you're launching a new product, securing international approvals, or strengthening your cybersecurity framework, Quality Commercial Consultants is your trusted partner for regulatory success.