Dr. Anna Schade has been working in the health sciences sector since 2015. Since 2021, she has been supporting customers worldwide as a qtec expert on regulatory topics such as the successful approval of medical devices and in-vitro diagnostics.
As a trainer, Dr. Schade educates IVD manufacturers, operators of in-house IVDs, authorities, and notified bodies at the qtec Academy on a wide range of topics including successful conformity assessment procedures and preparation of technical documentation for in-vitro diagnostics, requirements for in-house IVDs, and quality management system requirements according to IVDR, ISO 13485, and ISO 15189 / RiliBäk.
What matters most to her as a speaker: "Sharing knowledge, working together on solutions, implementing ideas: always different, always fresh, and always personal. Every topic is as individual as the participants. That makes it fun and exciting."
