Section: Lesson 2: The regulatory framework: definitions of Medical Devices and in vitro diagnostics (IVDs) | Introduction to Medical Devices and their regulatory framework | EUPATI Open Classroom

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Section outline

- Select activity 1. The European Medical Device Regulation (EU) 2017/745 (MDR)
  
  1. The European Medical Device Regulation (EU) 2017/745 (MDR) Page
  
  Learners must
  
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- Select activity 2. The European in Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 (IVDR)
  
  2. The European in Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 (IVDR) Page
  
  Learners must
  
  View
- Select activity 3. Additional Resources on MDR and IVDR
  
  3. Additional Resources on MDR and IVDR Page
  
  Learners must
  
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- Select activity 4. References
  
  4. References Page
  
  Learners must
  
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