QRT Consulting Group specializes in guiding small and medium-sized medical device firms through the complex regulatory landscape from inception to scale. Leveraging deep domain expertise in FDA, EU MDR, ISO standards (ISO 13485, ISO 14971, ISO 10993), and toxicology, QRT delivers hands-on support in regulatory compliance, quality systems, risk management, and M&A due diligence. Their approach not only identifies gaps and mitigates risk, but also builds implementation roadmaps customized to client operations and strategic business goals. With leadership by seasoned medical device professionals (e.g., President Heather Ferguson) and a reputation for collaborative, practical solutions, QRT accelerates compliance readiness and supports business growth.