Audrey Labèque

Audrey Labèque has a diverse and extensive background in the field of regulatory affairs and quality management within the medical device industry. Audrey'smost recent position was as the Quality and Regulatory Affairs Manager at inHEART, where they were responsible for developing and maintaining procedures within the company's quality management system (QMS), as well as preparing and maintaining regulatory approvals for its medical devices. Prior to this, they worked as a Consultant Manager at STRATEGIQUAL SAS, where they provided regulatory and quality support to pharmaceutical laboratories, medical device companies, and cosmetics companies. Audrey also gained experience at Graftys, a medical device manufacturing and distribution company, where they held various roles including Responsable Affaires Réglementaires & Biocompatibilité and Chargée d'Affaires Réglementaires. During their time at Graftys, they were involved in the elaboration and maintenance of technical documentation, management of regulatory relationships, and obtaining regulatory authorizations for medical devices in various markets. Audrey Labèque began their career as an Assistant in Regulatory Affairs at GRAFTYS and also gained experience as a Regulatory Affairs Intern. Audrey holds a Master's degree in Biomaterials and Medical Devices from the University of Bordeaux 1.

From 2009 to 2011, Audrey Labèque attended Université de Bordeaux, where they pursued a Master's degree in Biomatériaux et Dispositifs Médicaux. No specific field of study was provided.