Veronique Smith

Veronique Smith has extensive experience in regulatory affairs and clinical affairs in the medical device industry. Veronique has held various leadership positions in renowned companies such as Dentsply Sirona, Integra LifeSciences, KCI Medical, Teleflex Medical, Mentor Worldwide LLC, and Allergan.

At Dentsply Sirona, Veronique currently serves as the Vice President of Regulatory Affairs. Prior to this, they held the role of Vice President, Regulatory Affairs, Codman Specialty Surgical, at Integra LifeSciences. In this position, they led a team of 22 members and was responsible for developing and executing US and EU regulatory strategies.

At KCI Medical, Veronique held multiple roles including Senior Director, Regulatory Affairs and Clinical Affairs, Director, International Regulatory Affairs, and Senior Manager, Regulatory Affairs. Veronique managed the day-to-day activities of regulatory affairs specialists and supported the expansion of the company in core geographies.

During their time at Teleflex Medical, Veronique worked as a Senior Regulatory Affairs Specialist, preparing international regulatory submissions for medical devices and assisting with notified body audits.

At Mentor Worldwide LLC, Veronique served as a Senior Analyst, Global Regulatory Submissions, where they prepared international regulatory submissions for various medical products and assisted with regulatory issues during product design.

Veronique began their career at Allergan, where they held positions as a Clinical Research Supervisor and Research Associate. In these roles, they supervised data entry assistants, oversaw database entry for clinical studies, and liaised with investigators.

Throughout their career, Veronique has consistently demonstrated their expertise in regulatory affairs, managing international registrations, developing regulatory strategies, and leading teams.

Veronique Smith attended UC Santa Barbara, where they obtained a Bachelor's degree in Biological Sciences.