This seminar enables you to fulfill your (new) role as a medical device consultant in accordance with the Medical Devices Implementation Act (MPDG) and competently implement the legal requirements.
Our experienced experts will start by presenting the legal basis in Europe and the relevant changes introduced by the MPDG and the MDR. In doing so, they explicitly address the differences to the former Medical Devices Act (MPG) so that you understand the current requirements for the role of the medical device advisor precisely at the end.
After the seminar, you will be able to
The seminar meets the requirements of the MPDG for training as a medical device consultant. Upon passing a final written examination, you will receive a certificate attesting to this success and your participation.
You can find the exact learning content as well as the schedule of the seminar in the agenda: