e-Learning: Medical Device Advisor 83 MPDG - e-Learning in 5 modules for non-German speaking employees

- European Medical Device Law and its Application in Germany - Definition of a medical device is and how it is brought to market - Current Requirements and Tasks of a Medical Device Advisor - Vigilance / Market Observation (MD Monitoring and Reporting System) - Advertising Medical Devices to Healthcare ProfessionalsOur e-learning, specially tailored for medical device advisors, provides you with the essential knowledge to navigate your professional duties confidently and in full legal compliance.LernzieleMany medical device manufacturers, especially those with an international presence, have non-German speaking employees who inform or instruct GermanHealthcare professionals.- In order for the manufacturer to comply with the legal obligation to provide regular training, the Forum Institut offers an English-language e-Learning for medical device advisors.- Our e-Learning provides you with the latest legal requirements for medical device advisors - practical, concise, and flexible, at your own pace.- Upon successful completion of all modules and passing the knowledge assessments, you will receive a qualifying certificate. This certificate allows you to demonstrate your required expertise in accordance with83 MPDG to the relevant authority.- The certificate and assessments are generated on the basis of an automated, non-individual multiple-choice test.Zielgruppen- Do you advise healthcare professionals about medical devices or in-vitro diagnostics? - Does your employer need to demonstrate that you have been trained in accordance with83 MPDG? - Are you working in internal or external sales?- Then this online training is perfect for you. Acquire the required knowledge step by step - flexibly, at your own pace, and with full control over your schedule.