Instruction for Medical Product Consultants (EN)

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Target Audience
For all medical technology companies within the EU that want to train their employees according to European legislation in terms of the Medical Device Law Implementation Act (MPDG).

Level
Basics

Medical technology expert Hans-Jörg Gröber provides you with an overview of all legal requirements and roles in medical product consulting.

• Internalize the legal requirements, roles and responsibilities for your medical product company.
• Understand the basic qualifications that must be documented and demonstrated in the respective QA system.
• Learn everything you need to know about communication between internal and external business factors.
• Learn everything about risk assessment and the legal conditions for medical product manufacturing.

Basic course information

• Reinforce your understanding and knowledge with quizzes.
• In addition to the video content, you will receive practical supplementary materials.
• This course has automated subtitles. Your feedback helps us to continuously improve our offerings.

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