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Get to know your trainer  
Dr. Nadine Jurrmann holds a doctorate in biology and worked for a medical device manufacturer for over six years. Her responsi­bilities at that time included conducting clinical evaluations and…  
Learning Content  
Learning Content The seminar covers the following topics:  Regulatory basis according to MDR  Overview of different data routes (clinical data on your own device and equivalence data,…  
Learning Objectives  
Learning Objectives After the seminar, you will have all the relevant information to:  check and assess the qualifications of the service provider's authors based on reliable criteria. …  
Target Group      
Target Group     This seminar is designed for people who:  delegate the writing of clinical evaluations to service providers or internal departments and, therefore, must check that the…  
Requirements for Participation  
Requirements for Participation Participants can easily follow this seminar even without any special prior knowledge. Understanding your own medical devices is helpful.  
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…  
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 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.…  
Get to know your trainers  
Dr. Anja Kuhnert spent many years as a quality and regulatory affairs manager for various medical device manufacturers, where she gained first-hand experience of the concerns of start-ups and small…  
Get to know your trainers  
Lea Wettlaufer supports our customers in conducting clinical evaluations and post-market surveillance of medical devices. Her focus is on defining clinical strategies in accordance with MDR…  
Results 1271 until 1280 out of 1352
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