Our Training Course for Medical Device Consultants: For the Practical Implementation of the MPDG in Medical IT
Designed specifically for IT specialists in the healthcare sector and employees of IT departments at medical facilities (hospitals/clinics), this seminar offers more than just in-depth expertise on the significance and implementation of the Medical Device Act Implementation Act (MPDG). It bridges the gap between IT and medical technology and lays the groundwork for further in-depth application in day-to-day business.
During the 2-day event, participants receive intensive instruction and engage in a thorough examination of the contents of the Medical Device Law Implementation Act (MPDG). Technical questions are addressed, and in-depth expertise is imparted:
- What professional significance does the MPDG have for medical device consultants?
- What does the concrete implementation look like in terms of the tasks and duties of medical device consultants?
- What are the differences from the previous Medical Device Act (MPG)?
More than just a training course: The MPDG in the day-to-day work of medical device consultants
Of course, compliance with and ensuring electrical safety through initial and periodic inspections, as well as European standards and regulations, are important components of our continuing education event. However, we also aim to establish a clear connection to proper handling in the day-to-day work of medical device consultants: Topics such as rights, obligations, and liability arising from delivery and installation in the healthcare sector are therefore discussed in equal depth.
With this seminar, we at Baaske Medical aim to provide participants with a solid foundation of knowledge for further application in their day-to-day work.
Excerpt from the seminar content on Medical Device Consultants IT
- Medical Device Regulation (MDR)
- Updates on the Operator Regulation
- Risk Assessment
- Medical Device Adaptation Act (MPEUAnpG)
- Fundamentals of the Medical Device Law Implementation Act (MPDG) as the German supplement to the MDR 2017/745
And new:
- Qualification Options for Medical Device Consultants
- Radiation Protection Law
- EU/National Law
- Radiation Protection Regulation
- Electrical Safety in the Patient Environment
- Risk Assessment of Systems
- Medical IT / Medical Networks
- Data Protection / Patient Rights
Certificate
The training program for medical device consultants thoroughly prepares participants for a subsequent final exam. Upon successful completion of the exam, a personalized certificate covering the course content taught and tested in this seminar will be issued. Together with the regular, product-specific training conducted separately by the medical device manufacturer, our seminar provides the foundation for demonstrating expertise as required by Section 83 of the Medical Device Law Implementation Act (MPDG) and the MDR.
Dates
- Thu, Oct 8 – Fri, Oct 9, 2026
Seminar fee
Price: 600.00 € per person plus VAT.
Includes meals and dinner with an expert roundtable
Exclusively for Baaske-Medical customers
1 or more people: 550.00 € plus VAT
3 or more people: 520.00 € per person plus VAT
5 or more people: 500.00 € per person plus VAT
Venue
Seminar Rooms
Baaske Medical GmbH & Co.KG
Bacmeisterstraße 3
32312 Lübbecke, North Rhine-Westphalia
Upon request, we will be happy to arrange suitable accommodations for the duration of your stay; however, please note that the cost of accommodations is not included in the price.
Login