Judith Koehnen is Director Project Management of Covance’ Device and Diagnostic Solutions Business Unit. She has 24 years industry experiences with over 21 years in the CRO environment and over 16 years in the Medical Device arena.
Judith has been in leadership roles in Project Management and the Medical Device Business unit. She has been responsible for Global Medical Device Training initiatives across all functions at Theorem and Chiltern now Covance and SOP revision in order to comply with Medical Device requirements and terminology across the globe. Currently she is leading the trainings initiative for the upcoming Medical Device and In-vitro Diagnostic Regulation.
From 2012 – 2015 Ms. Köhnen was co-chair and from 2015 – 2016 chair of the European CRO Federation Medical Device Working Group.
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