Seminar Medical Device Consultant MPDG

Get certainty about the tasks and duties you will face in the future

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. 

Learn to implement the legal requirements in practice competently

After the seminar, you will be able to 

• apply your newly acquired knowledge in a targeted manner when advising and selling medical devices, 
• recognize serious incidents in the context of market surveillance and report them accordingly, and
• interact skillfully with other roles in the company, such as the Person Responsible for Regulatory Compliance (PRRC). 

A certificate attests to your newly acquired skills as a medical device consultant

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: