Webinar medical device consultant according to §83 MPDG with certificate

A medical device consultant is a person who provides healthcare professionals with specialist information about medical devices or instructs them in their proper use, in accordance with § 83 MPDG. The requirements, tasks and responsibilities are precisely defined in the Medical Devices Directive Implementation Act (MPDG). It is mandatory for all employees with customer contact (including office staff and service) if they provide information or instruction on the company's products.

The MPDG stipulates that medical device consultants must undergo regular training.

In addition to fulfilling legal requirements, medical device consultants with knowledge of the background can better advise their customers and thus contribute to the company's success. Knowledge of regulatory procedures and compliance with them minimises risks for the company and thus supports the long-term success of the company.

The seminar covers the Medical Device Regulation (MDR) in detail.

The seminar will cover the current status of implementation of the new Medical Device Regulation (MDR), changes and challenges.

With many examples from the approval and distribution of medical devices, the „dry“ subject matter is conveyed clearly and gives the participants practical knowledge for their daily work with customer contact.

After the webinar and passing the test, all participants receive a certificate according to §83 MPDG.

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