Dan Miller
About Dan Miller
Dan Miller serves as the Vice President of Regulatory Affairs, Clinical Affairs, and Quality Assurance at Sonendo, Inc., a position he has held since 2012. Previously, he worked for seven years as the Director of Regulatory Affairs and Quality Assurance at Smith & Nephew.
Work at Sonendo
Dan Miller has served as Vice President of Regulatory Affairs, Clinical Affairs, and Quality Assurance at Sonendo, Inc. since 2012. In this role, he oversees the regulatory compliance and quality assurance processes critical to the company's operations. His leadership contributes to the development and implementation of strategies that ensure product safety and efficacy within the medical device sector.
Previous Experience at Smith & Nephew
Prior to his tenure at Sonendo, Dan Miller worked at Smith & Nephew as the Director of Regulatory Affairs and Quality Assurance from 1993 to 2000. During this seven-year period, he was responsible for managing regulatory submissions and ensuring compliance with industry standards. His experience at Smith & Nephew provided him with a strong foundation in regulatory processes and quality management.
Regulatory Affairs Expertise
Dan Miller possesses extensive expertise in regulatory affairs and quality assurance, developed over his career spanning multiple decades. His knowledge encompasses the regulatory landscape for medical devices, including compliance with FDA regulations and international standards. This expertise is vital for navigating the complexities of product approvals and maintaining quality management systems.
Career Timeline
Dan Miller's career includes significant roles in regulatory affairs and quality assurance. He began his professional journey at Smith & Nephew, where he spent seven years in a leadership position. Since 2012, he has been with Sonendo, Inc., accumulating over 12 years of experience in his current role. His career reflects a commitment to regulatory excellence and quality management in the medical device industry.