Dr Delphine Huser

Senior Associate

Delphine is a regulatory and clinical affairs medical biologist, with a research expertise spanning from fundamental to applied research.
Some of the scopes of Delphine’s activities as a Senior Associate in Regulatory and Clinical Affairs are Clinical investigations for both CE-marked and investigational devices, clinical evaluation reports, realization and improvement of technical files, registration of medical devices and QMS deployment.
Within Medidee, Delphine is responsible for managing the Clinical Investigation services delivery Process and assuring its overall compliance with Good Clinical Practice requirements (ISO 14155 and ICH E6 [R2]) related to quality and regulatory aspects.
Delphine speaks French and English.