EU Medical Device Regulatory Affairs explained Simply free download

EU Medical Device Regulatory Affairs module explains how Medical Device Regulation works in the European Union . This module is ideal for a person who wants to work in medical device regulation . If you are a medical device manufacturer outside the EU and would like to sell your product in Europe this course is perfect for you. You will understand how important the ISO 13485 2016 standard is to gain market approval. If a student wants to understand the rules that govern the sale of medical devices in the EU market place this course will be ideal for you . Each lecture is explained in a simple format. If the student takes each lecture step by step, they can understand how a company gains permission to manufacture .Authentication failed. Unique API key is not valid for this user.

Who this course is for:

  • Medical Device Engineers
  • Quality control within the medical device industry
  • Operation Managers within the medical device industry
  • Entrepreneurs in setting up medical device technologies.
  • Quality Control Technicians
  • Process Engineers
  • Quality Control Engineers
  • Regulation
  • Marketing within the medical device industry.
  • Research and Development Engineers within the Medical device industry
  • Students in Biomechanical Engineering.
  • Students in Pharmaceutical science.
  • Students in Regulation affairs.
  • Students in Quality Assurance and quality control.
  • Internal and external audits of the medical device Industry
  • Medical device manufacturers inside and outside of Europe.
File Name :EU Medical Device Regulatory Affairs explained Simply free download
Content Source:udemy
Genre / Category:Business
File Size :4.19 gb
Publisher :Martin Conneely
Updated and Published:05 May,2022

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File name: EU-Medical-Device-Regulatory-Affairs-explained-Simply.rar
File Size:4.19 gb
Course duration:7 hours
Instructor Name:Martin Conneely
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