e-learning: Refresher Medical Device Advisor §83 MPDG - e-Learning in 3 modules for non-German speaking employees
Our 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.
- European Medical Device Law and its Application in Germany
- Current Requirements and Tasks of a Medical Device Advisor
- Vigilance / Market Observation (MD Monitoring and Reporting System)
| Veranstaltungs-Code | FB24-526381-61076890 |
Bildungsziel der Schulung:
Many medical device manufacturers, especially those with an international presence, have non-German speaking employees who inform or instruct German Healthcare professionals.
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In order for the manufacturer to comply with the legal obligation to provide regular training, the Forum Institut offers an English-language e-learning course for medical device advisors.
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Our refresher e-learning provides you with the latest legal requirements for medical device advisros - practical, concise, and flexible at your own pace. This e-learning is designed for anyone whose last training for medical device consultants in accordance with § 83 MPDG was no more than three years ago.
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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 with § 83 MPDG to the relevant authority.
Veranstaltungsort:
Online-Webinar
weitere Orte/Termine
Kursart:
Online-Webinar
Kostenlos Info anfordern
