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MedTech Summit


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10 - 14 June 2024
DoubleTree by Hilton Brussels CityBrussels, Belgium (Hybrid Event)

Carmen Giefing-Kröll
Advanced Clinical Evaluations Manager at MED-EL


Carmen Giefing-Kröll started her professional career in medical device industry at MED-EL over 7 years ago. There she is responsible for clinical evaluations of medical devices from class I to class III under MDR and AIMDD, providing substantial input for the post market follow-up activities according to the clinical development plan. In addition, she is experienced in compiling the clinical documentation for worldwide submissions including NMPA (China) and FDA.

Carmen holds a doctoral degree in Biotechnology. Before joining the medical device field, she has worked for 10 years in vaccine industry focusing on bacterial antigen and antibody research. She further gained experience in immunology and aging at Institute for Biomedical Aging Research of the University of Innsbruck.

Agenda Sessions

  • Planning the Perfect Post Market Clinical Follow-Up (PMCF) & Post Market Performance Follow-Up (PMPF)