Laure A.

With an engineering background in physics and a 26-year career at Advanced Bionics, where I most recently served as Senior Director of Global Clinical Research, I possess extensive experience in international management of clinical teams in the field of Class III medical devices, particularly cochlear implants (ENT sector). These are complex systems integrating an implanted component, an external processor, and adjustment software. My expertise notably covers clinical regulatory affairs, clinical development, scientific marketing, and the valorization of scientific data.

Throughout my career, I have operated at the interface between industry, academia, hospitals, and CROs, allowing me to deeply understand the challenges and constraints of each stakeholder.

I founded LPA ClinEthica to support MedTech companies in achieving their clinical objectives, including clinical strategy, regulatory submissions (EU MDR, US FDA, NMPA China), clinical study implementation, post-market activities, scientific engagement with healthcare professionals, and data valorization.

I am convinced that a clinical strategy is only valuable if it is not only compliant but also grounded in reality: feasible, credible, and capable of generating robust and actionable data.

I offer flexible support based on needs, from one-off assignments to regular or long-term engagements, in both French and English.