EU MDR Regulation 2017/745 - Essential Awareness Exam

Self Assess and improve your knowledge on the essentials of EU MDR 2017/745 which is going to be enforced on May-2020

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EU MDR Regulation 2017/745 - Essential Awareness Exam

What You Will Learn!

  • Self assessment on EU MDR Knowledge
  • Empower to acquire fundamentals EU MDR

Description

Value Addition Alerts:

  1. Passing Certification Awarded By Instructor

  2. Road Map for Further Learning

Certification: Udemy does not provide certification for exams, they only do in the case of Video Courses. But the great news here is, we have empowered our paid students to have a certificate, once they qualify by 80% in the exams. It is a manual process, in which learners our requested to submit evidence of qualification, and apply for the certificate. The certificates are issued at the end of a month.

----------------------------------------------------------------------------------------------------------------------------The European Medical Device Regulation (MDR) is a novel collection of regulations that encompasses the manufacturing and distribution of medical devices instruments in Europe, and fulfillment of the regulation will be mandatory for medical device companies after the enforcement for all those companies who want to sell their devices in the markets of European countries. Now the companies need individuals who are well trained and competent regarding the new requirements of EU MDR.

The practice exam is made envisioning this issue, to help delegates self assess themselves on essential changes in the new regulations. After the individuals complete one practice test, they can review their answers with the textual explanation provided by the Instructor.

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Exam Composition

You will be assessed when you take this online exam in following areas (Course Objectives):

  • The Classification of Medical Devices

  • The Rules of the MDR

  • Important definitions regarding device exposure

  • Unique Device Identifier

  • EUDAMED

  • Sub-classification of Class I

  • New Products incorporated under the scope of new MDR

  • Enforcement and Publication Timelines of the New MDR

  • MDR Versus MDD

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Food for Thought

Be Familiar with EU MDR Regulation knowledge which you hold...

If you think you are an expert in EU MDR Regulation after taking courses on the subject and working with Quality Systems...

You need to hold on!

Join this exam and self assess yourself!

Maybe you need to learn and learn...

Or you can prove your knowledge and expertise by successfully completing this exam.

Both ways, you are in a win-win situation.

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Good news: We will be adding more content for example case studies to practice tests in the future. If you feel that you lack the knowledge you can take  EU MDR Regulation courses from Udemy or the instructor to guide you on gaining  EU MDR Regulation knowledge.

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EU MDR Regulation File: The regulation is published in Official Journal of the European Union. One can view and obtain it online, if you are facing any difficulties, the instructor can help you to have that document. 

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One Month Money Back Guarantee: Don't forget One Month 100% Money Back Guarantee without inquiry. This means you have unconditionally no risk when registering to this Course.

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Ask Questions & Report Complaints: Discussion forum on the right side of this course can be used to discuss specific queries and report problems you are facing about the content of the course.

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Take this course: Follow the “Take This Course" Button by clicking at the Top Right Hand Side of the Page. Proceed with the instructions and follow it to register and pay for the course.

Who Should Attend!

  • Medical Device Professionals in Europe
  • Quality Professionals in the medical device sector
  • Individuals looking to learn EU MDR
  • Compliance Professionals in Europe

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Tags

  • Medical Device Development

Subscribers

64

Lectures

0

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