The Funke Medical AG supports dealers and users by implementing the legal requirements of the European Medical Device Regulation (MDR). In a free online seminar of Funke Medical AG, interested parties will learn worth knowing facts about the most important innovations according to MDR 2017/745.
Funke Medical also offers the necessary certificate courses.
From 26th May 2021, the new regulation will entail many mandatory changes for the healthcare sector that go beyond the existing national and European directives for medical devices. The aim of the MDR is to unify regulations within the European Union, to ensure a well-functioning internal market for medical devices and to establish high and consistent quality standards in order to ensure patients and users a safe product. The far-reaching effects of the MDR require manufacturers of medical devices as well as distributors to prepare for the requirements in time.
All products of the Funke Medical AG, manufacturer of decubitus therapy systems, have been compliant with the new legal guidelines since 2017. Familiar with the topic, the company supports the current need for action in the health sector with a free, subject-specific online seminar. The aim is to communicate the most important changes in the field of decubitus supply with class I products.
The Funke Medical Academy not only conveys knowledge for all professions in the healthcare sector. As a part of the compulsory continuing education, it also offers the necessary certificate courses. All courses content is based on a didactically thought-out concept that always reflects the latest state of science and is open to Funke Medical AG customers and cooperation partners.