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1352 Search result(s):
Target Group      
Target Group     This seminar is designed for individuals who:  are responsible for implementing the requirements of the UDI system in accordance with MDR.  are entrusted with the…  
Learning Objectives        
Learning Objectives       After the seminar, you will be:  familiar with the basic regulatory requirements relating to the UDI system.  able to identify the requirements applicable to…  
Learning Content  
Learning Content The seminar covers the following topics:  Regulatory requirements  Concept of the basic UDI-DI  Assignment and allocation of the UDI (GS1 and HIBCC) …  
Get to know your trainer  
Dr. Bernhard Gerstenecker has a PhD in microbiology and has spent his entire professional life in the medical device industry dealing with all aspects of IVD systems. For around 25 years, he…  
What happens if questions or problems arise?  
What happens if questions or problems arise? If you experience technical problems while participating or have any other questions, you can contact our support team anytime, even at short notice. The…  
How is the seminar conducted?   
How is the seminar conducted?  The seminar takes place either in person or online.   Our online/remote seminars and workshops are conducted via the video conferencing tool MS Teams. We…  
What happens after registration?  
What happens after registration? After registering, you will receive a confirmation email containing the meeting link, the time, and information about the participants.   An invoice will be…  
Requirements for Participation  
Requirements for Participation Knowledge of the regulatory requirements of the MDR and IVDR is helpful.  However, participants can also attend this seminar without detailed prior knowledge; it…  
Target Group      
Target Group     This seminar is designed for:  people who professionally inform users from specialist circles about medical devices  people who professionally instruct users from…  
Learning Objectives    
Learning Objectives   After the seminar, you will know:    the requirements of the MDR/IVDR  the detailed tasks and duties of a medical device consultant  the qualification…  
Results 1301 until 1310 out of 1352
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