Sarah Koch is a Regulatory Affairs Manager with extensive experience in the medical device industry. Currently at Lohmann & Rauscher since March 2019, Sarah focuses on the creation and maintenance of technical documentation for active and non-active medical devices of risk classes I-IIb and oversees conformity assessment procedures in compliance with MDD and MDR during development projects and product modifications. Previously, at heyer medical AG from March 2016 to February 2019, Sarah managed the maintenance, development, and implementation of the Quality Management System according to ISO 13485 and 9001, while also preparing and conducting internal audits. Sarah holds a Master of Science in Health Economics from the University of Cologne.
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