2026-03-21 2026-03-21 , online online, 390 € zzgl. MwSt. e-Learning: Medical Device Advisor §83 MPDG

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.

Themen
  • 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 Professionals


Who should attend
  • 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 with § 83 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.
Ziel der Veranstaltung
Many medical device manufacturers, especially those with an international presence, have non-German speaking employees who inform or instruct German Healthcare 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 with § 83 MPDG to the relevant authority.

The certificate and assessments are generated on the basis of an automated, non-individual multiple-choice test.
Teilnehmerkreis

After completing this course, you will be optimally prepared:

  • You will understand the regulations for medical devices (MDR and IVDR) and your responsibilities and obligations as a medical device advisor in accordance with § 83 MPDG.
  • Practical tips will simplify the implementation of your reporting and compliance duties.
  • Additional insights will support you in your day-to-day work, particularly when collaborating with healthcare professionals.

e-Learning: Medical Device Advisor (MPDG)

Medical Device Advisor §83 MPDG

e-Learning in 5 modules for non-German speaking employees

Benefits
  • Up-to-date expert knowledge
  • Flexible learning at your own pace
  • Qualifying certificate
  • Practical examples and case studies
  • Official certification according to ISO 9001 and ISO 21001

Webcode 26122537

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Alles auf einen Blick

Termin

anytime

anytime

Zeitraum

online

online
Veranstaltungsort

online

online

Downloads
Gebühr
Your contact

Verena Planitz
Conference Manager

+49 6221 500-655
v.planitz@forum-institut.de

Details

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.

Themen

  • 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 Professionals


Who should attend
  • 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 with § 83 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.

Ziel der Veranstaltung

Many medical device manufacturers, especially those with an international presence, have non-German speaking employees who inform or instruct German Healthcare 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 with § 83 MPDG to the relevant authority.

The certificate and assessments are generated on the basis of an automated, non-individual multiple-choice test.

Teilnehmerkreis

After completing this course, you will be optimally prepared:

  • You will understand the regulations for medical devices (MDR and IVDR) and your responsibilities and obligations as a medical device advisor in accordance with § 83 MPDG.
  • Practical tips will simplify the implementation of your reporting and compliance duties.
  • Additional insights will support you in your day-to-day work, particularly when collaborating with healthcare professionals.