According to the legal definition, medical device consultants are all persons who inform or instruct professionals, about medical devices.
To be able to work as a medical device consultant in sales and service, it is important to have the necessary expertise and to be able to prove this to the authorities. The legal basis for this is Section 83 (3) of the German Medical Devices Implementation Act (Medizinprodukte-Durchführungsgesetz, MPDG). You will learn about the concrete rights, tasks and obligations associated with this in our individual manufacturer-specific training courses. BEO BERLIN provides a practical experience in online or classroom training courses incorporating product and company-specific basic knowledge with many practical examples, which is needed for the role as a medical device consultant.
Our training courses covers the following topics:
- Legal basics
- Classification and evaluation rules and examples
- Labeling and product documentation of medical devices
- Elements of technical documentation according to MDR
- Tasks in the context of Market Surveillance
- Distinctions to other persons and duties
- Introduction to the reporting system
- Examples of the information flow
The training is suitable for individuals, small and large groups. The content is relevant for newcomers as well as experienced medical device consultants wanting to refresh existing knowledge. Through the product and company specific design you will learn what you need without the often irrelevant ballast of details pertaining to other product classes. After successful participation, attendees receive a certificate that is suitable as proof of qualification for presentation to authorities and for enhancing their personal resume.
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