Lisa Isernhinke has been active in the healthcare sector since 2013 and has extensive experience from pharmaceutical practice in public pharmacies. Since 2024, she has been working at qtec Services, supporting clients worldwide as an expert in toxicology, biocompatibility, and regulatory requirements related to combination products, including GMP compliance.
As a trainer at the qtec Academy, she conveys practical and understandable knowledge about biocompatibility and toxicology to manufacturers in the medical device and pharmaceutical industries.
What matters most to her as a speaker: "I especially enjoy conveying knowledge in a way that enables participants not only to understand the requirements but also to independently implement their tasks. From my own work experience, I know how challenging it is to transfer complex regulations into daily practice. That is why my seminars emphasize practical applicability, concrete implementation, and providing participants with real tools."
