Anne Kroker

Resposible for clinical trials, analyzation and publication of study results, responsible for all kind of questions concerning certifcation according to DIN EN ISO 13485, MEDDEV 2.7.1, DIN EN ISO 14155, regulatory affairs, risk management and change management of the medical devices, managing post-market surveillance studies

Resposible for clinical trials, analyzation and publication of study results, responsible for all kind of questions concerning certifcation according to DIN EN ISO 13485, MEDDEV 2.7.1, DIN EN ISO 14155, regulatory affairs, risk management and change management of the medical devices, managing post-market surveillance studies

Plan, manage and coordinate development of a medical device according to DIN EN ISO 13485, DIN EN ISO 14971, MEDDEV 2.7.1, etc, leading a team of interdisciplinary and external researchers, physicians, engineers and other specialists

Halten von Vorlesungen, Seminaren und Praktika, Forschung auf dem Gebiet der Emissionsspektroskopie an Gläsern, Leitung der Weiterentwicklung eines Laborverfahrens bis zum Einsatz in der Industrie

Biomaterialien, Qualitätsmanagement