Kira Meyerovich is an accomplished professional in the field of regulatory affairs and policy within the medical technology sector. Currently serving as Co-Chair of the Regulatory Affairs Committee for In Vitro Diagnostics at MedTech Europe since June 2022, Kira has also held the position of Regulatory Affairs Manager for Advocacy at BD since April 2020. Kira contributes to international standardization as Vice Convener and Convener of ISO/TC 212 WG 3 since September 2018 and has previously managed regulations and industrial policy at MedTech Europe from August 2016 to April 2020. Kira's early career includes editorial roles at De Gruyter and research at the ULB Centre for Diabetes Research, complemented by foundational experience as a Quality Manager Assistant at PHOENIX Pharmahandel GmbH & Co KG. Kira holds a Ph.D. in Biomedical and Pharmaceutical Sciences from Université libre de Bruxelles and a Diplome in Cell/Cellular and Molecular Biology from The University of Freiburg.
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