Cécile Vedrenne

Cécile Vedrenne has had a diverse range of work experiences. Cécile began their career as a Research Scientist at the Biozentrum, University of Basel, where they worked from January 2001 to March 2007. Following this, they joined Novartis Consumer Health as a Regulatory Affairs Specialist from October 2007 to April 2008. From there, they gained extensive regulatory affairs experience at B Braun Medical, starting as a Regulatory Affairs Junior Manager from November 2008 to January 2010, then as a Regulatory Affairs Manager from January 2010 to October 2014. Cécile'sresponsibilities at B Braun Medical included regulatory activities related to pharmaceutical production, worldwide registration of Hospital Care products, and regulatory activities linked to Medical Devices of Class I to III. Finally, since December 2014, Cécile has been at Accuray International, where they initially served as a Regulatory Affairs Manager until October 2015. Cécile then took on the role of Senior Regulatory Affairs Manager, responsible for the registration of radosurgery and radiotherapy Medical Devices in EIMEA, as well as the management of post-market surveillance activities. In addition, they supervised HSE and radiation safety compliance in EIMEA.

Cécile Vedrenne received their PhD in Biological and Medical Sciences from the Université de Bordeaux between 1996 and 2000.