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Dallas L. Thomas holds a Master's degree in Health Administration and a Master's degree in Public Administration from the University of Utah. Currently serving as a Consultant at IQVIA, Dallas specializes in pharmaceutical and medical device regulations, focusing on FDA 483 regulatory compliance and CGMP audits. Previously, Dallas operated as Principal Regulatory Affairs Consultant at Thomas Regulatory Resolutions, Inc. and has extensive experience in the medical device sector, which includes authoring product submissions under EU MDR regulations and conducting audits. Competent in regulatory strategies, Dallas has contributed to various companies such as MicroVention-Terumo, Medtronic, and Telos Partners, enhancing compliance and quality assurance. Dallas is also a Certified Lead Auditor in ISO 13485:2016 for medical devices.