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Get to know your trainers  
Andreas Kalchschmid-Lehmann is an expert in QM and in vitro diagnostic medical devices with more than 17 years of practical experience. He is the author of the book “ISO 13485 – Chance statt Hürde”…  
Get to know your trainers  
After completing her studies, Claudia Volk gained several years of experience as a quality and regulatory affairs manager in a regulated environment, initially in food production and later as a…  
Learning Content  
Learning Content The following topics are covered in the seminar: Basics Definition of quality, objectives of quality management  Role of ISO 13485, also in the context of MDR …  
Learning Objectives  
Learning Objectives After the seminar, you will be able to:  understand and confidently interpret ISO 13485:2021.  distinguish between requirements that are mandatory and those that are…  
Target Group  
Target Group This seminar is designed for career starters and career changers who (in the future) will take on one or more of the following roles:  Quality Manager  Quality Management…  
Requirements for Participation  
Requirements for Participation The seminar is aimed explicitly at young professionals and career changers. Participants can, therefore, follow this seminar easily, even without any special prior…  
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. The…  
Get to know your trainer  
Dr. Anja Kuhnert is a highly qualified regulatory and quality affairs expert with more than ten years of experience bringing medical devices to market. She is well versed in implementing and…  
Results 1231 until 1240 out of 1352
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