Denis Klopfenstein started off his career as an electronics and embedded software engineer. He rapidly moved on to the Medical Devices industry where, over 20 years, he has held positions ranging from project management to R&D direction. He brings to EspeRare his expertise in the development and industrialisation of medical devices, as well as regulatory affairs and product certification expertise.
At EspeRare, Denis is responsible for building up and implementing all quality certifications and regulatory work relating to the FloWatch market relaunch.
Regulatory & Medical Devices Consultant
As a private non-for-profit organisation, we strive to uncover the potential of existing molecules to address severe therapeutic unmet needs in rare diseases, thus giving better chances to existing drugs to reach these underserved patients.