e-Learning: Medical Device Advisor (MPDG) - according to § 83 MPDG: Training and e-Learning for non-German speaking employees - E-Learning von FORUM Institut für Management GmbH

- European medical device law and its application in Germany - The MDR and IVDR - an overview of all relevant innovations for medical device advisors - What a medical device is and how it is brought to market - Current requirements and tasks of medical device advisor - Vigilance and market observationWith our e-learning specially tailored to medical device consultants, you will receive the knowledge essential for medical device advisors - so that you can move about in your everyday professional life with legal certainty!

Our e-learning is perfectly tailored to medical device advisors: Learn which current legal requirements are placed on medical device advisors.- The focus of the 5 modules is on the regulatory framework for medical devices in the European Community and the current requirements and duties of medical device advisors. - After successful completion of this e-learning, you will be familiar with the legal framework and will be ideally equipped for your day-to-day work as a medical device advisor.

- You inform professionals about medical devices or in vitro diagnostics and are a medical device advisor? - Your employer has to prove that you have trained according to § 83 MPDG? - You are a member of the internal or external sales force? - Then you are in the right place. With this online training you can get the necessary knowledge step-by-step at your own learning pace with free time management.