Seminar Risk Management and ISO 14971 (two days)

Become the first point of contact for risk management in your company 

This seminar will not only provide you with a comprehensive knowledge of risk management but also the capability to coordinate the required activities in your company and compile compliant risk management files for your medical devices.

Seminaranmeldung: Institut für IT im Gesundheitswesen

Registration for the seminar Risk Management and ISO 14971 (English)

After your registration you will directly receive a booking confirmation with further details. After the confirmation you are bindingly registered, but you can name another person as a substitute at any time.


Seminar details

Risk Management and ISO 14971 (English)
11.10 - 12.10.2023 each from 09:00 until 17:00 o'clock (MEZ - MESZ)
Online Seminar

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PS: Would you like another appointment? Get in touch with us! Or consider an In-house seminar .

Gain the required knowledge to create audit-proof documentation and to defend it competently 

You will first become familiar with all relevant laws, standards, directives, and regulations, as well as their interaction in the context of risk management. This will provide you with the basis for optimally implementing your company's required risk management processes and creating a complete risk management file for your medical devices. 

Carry out risk management processes in a targeted and efficient manner in your company 

We will introduce you to the most suitable methods and approaches for risk analysis, risk acceptance, and risk minimization.
You will be able to 

  • define (un)acceptable risks for your medical devices, 
  • systematically identify hazards from your medical devices, 
  • successfully manage the risks posed by your medical devices, and 
  • integrate these activities into your development process in a meaningful way. 

Benefit from our many years of experience to get started quickly

Our seminar has matured over many years so that the content is optimally tailored to the needs of the participants. In addition to the clearly structured lectures and descriptive documents, you will benefit from numerous case studies and practical exercises. You will also receive useful tips to prevent problems in audits and during the approval of your medical devices. 

You can find the exact learning content as well as the schedule of the seminar in the agenda:

Download Agenda (PDF)

Note: There is a voluntary online exam at the end of the seminar (duration: approx. 20 min). By passing this exam, you will receive a certificate proving your newly acquired knowledge and skills in addition to your attendance confirmation.



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