Dallas L. Thomas, a Regulatory Affairs Consultant and Certified Lead Auditor, has built a career providing guidance and training to medical device companies across the US and internationally. With a Master's degree in Health/Health Care Administration and Management and a Master's degree in Public Administration, along with years of experience in the field, Thomas has worked with low to high-risk medical devices, including dental, neuro-surgical, vascular access, ultrasound, stent grafts, sutures, ophthalmic and vision care, biosensors, and wound care. He takes a lean approach to reduce costs and provides the most robust regulatory, compliance, and quality solutions for his clients. As a hands-on strategy developer, he believes in open dialogue, mutual input, and upholding relationships with his clients by being transparent and approachable. Thomas is the Principal Regulatory Affairs Consultant, Quality Consultant, Auditing & Compliance & Training FDA at Thomas Regulatory Resolutions, Inc. and was a contract medical device regulatory affairs and quality consultant at Telos Partners prior to this.