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Requirements for Participation  
Requirements for Participation Participants can easily follow this workshop even without any special prior knowledge Please note that, for licensing reasons, we are unable to provide participants…  
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. Within the next 48 hours, you…  
How is the workshop conducted?  
How is the workshop conducted? Our online/remote workshops are conducted using the MS Teams video conferencing tool. We recommend that you dial in 20 minutes before the start of the workshop to…  
Learning Content  
Learning Content Advantages of structured data for regulatory tasks YAML files: use cases, creation, validation JSON files: use cases, creation, validation JSON schema files: use cases,…  
Learning Objectives  
Learning Objectives Be able to name the advantages of structured data (e.g. in YAML and JSON format) in the creation, review and submission of technical documentation Be able to explain the…  
Target Group  
Target Group The workshop is aimed at employees of medical device and IVD manufacturers as well as notified bodies who create or review technical documentation in accordance with laws and…  
AI Experiment Technical Documentation  
Dear colleagues in medical technology, …  
EN_Seminar Internal Auditor Medical Devices according to ISO 19011  
This seminar will provide you with the necessary competencies to perform effective audits as an internal auditor in your company.  
Seminar Internal Auditor Medical Devices according to ISO 19011  
This seminar will provide you with the necessary competencies to perform effective audits as an internal auditor in your company.  
AI-Tech  
AI Technology for Medical Technology Our solutions for your digital transformation …  
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