How to get approval to sell your Medical Devices within the European Union. Rules explained in simple format for student
Master key concepts and practical skills through structured learning modules. By completing this curriculum, you'll gain valuable expertise applicable to real-world scenarios.
Understand how Medical Device Regulation works in the European Union.
Differentiate between a regulation and a directive.
Steps required to gain permission to manufacture and sell a medical device in the European Union.
Explain the roles and responsibilities of a Competent Authority & a Notified Body with regard to European Union regulation.
Understand in simple terms the Active Implantable Medical Device Directive 90/385/EEC.
This comprehensive European Medical Device Regulation explained in Simple terms curriculum is designed to take you from foundational concepts to advanced implementation. Each module builds upon the previous, ensuring a structured learning path that maximizes knowledge retention and practical application.
Understand what you need to succeed in this course and determine if it's the right fit for your learning goals
What you need before starting this European Medical Device Regulation explained in Simple terms course:
This course is perfect for:
Everything you need to know about this online course, from duration to certification
Course Instructor
Martin Conneely
Expert instructor with industry experience
Course Language
English
All materials in English
This online course offers comprehensive training with expert instruction, practical exercises, and a certificate of completion. Join thousands of students advancing their careers through quality online education.
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