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Learning Content  
Learning Content The course covers the following topics:  Regulations: MDR, MEDDEV 2.7/1 rev. 4, IMDRF MDCE WG/N56FINAL:2019, MDCG 2020-13  PICO, PRISMA, and other methods …  
Learning Objectives  
Learning Objectives After the course, you will:  be familiar with the regulatory requirements for systematic literature searches.  be able to conduct systematic literature searches not…  
Target Group  
Target Group This course is designed for:  Clinical Evaluators  Medical Writers  
Requirements for Participation  
Requirements for Participation Participants can easily follow this course 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 and information about the participants.      An invoice will be sent to…  
How is the course conducted?  
How is the course conducted? The course consists of the following components:  Access to our e-learning platform  One task course each for literature research and literature evaluation…  
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. 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:  Definition and categorization of the PMS process within the overall technical documentation process and the QMS  Regulatory…  
Learning Objectives  
Learning Objectives After the seminar, you will: know the definition and categorization of the PMS process within the overall technical documentation process.  know the regulatory basis for…  
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