From concept, through design and commercialization, Pathway Regulatory Consulting, LLC provides regulatory and quality solutions for manufacturers seeking to market Medical Devices in the United States, Canada and the European Union.

We provide a wide range of services from Regulatory strategy and submission to Quality Management System support. Services include: 510(k), pre-IDE, technical file development, Canadian licenses, design controls, risk managment, quality system audits, labeling, advertising and other compliance reviews.