Laboratory technician, clinical chemistry (1994)
Louisa Memborg is part of the Medical Device RA & QA Team. She has in-depth knowledge of the regulatory requirements for medical devices, which also covers experience with development and market authorizations in relations to various technologies ranging from wound care and general surgery devices to electronic devices, software and medical APPs.
Louisa has experience with defining regulatory strategies for medical devices in EU, ASIA, South America and the US.
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