Nevi Zorgcongres 2020
6 februari 2020, Van der Valk Hotel Utrecht

Jenny Wennerberg, Essity

Global Regulatory Affairs Director, Essity

Jenny Wennerberg, Essity

Extensive global experience in the field of Regulatory Affairs and Quality Assurance for Medical Devices with more than 15 years in different roles for companies such as Essity, Dentsply and XVIVO Perfusion. As Global Regulatory Affairs Director, Regulatory Excellence, Jenny is responsible for ensuring MDR requirements are fully understood within the organization, that there are procedures in place to define the compliance work and together with all other team members of the MDR project responsible to ensure that all devices within Essity┬┤s assortment will be compliant with the new Medical Device Regulation (MDR) within the given timeframe. One special area of interest is the implementation of the new Unique Device Identification (UDI) requirements and EUDAMED and Jenny is a member of the UDI and EUDAMED workstream of MedTech Europe. Jenny holds a M.Sc. in Mechanical Engineering.

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