ISO13485: 2016 - Quality Management Systems for Medical Devices

  • Tuesday
  • June
  • 15
  • 2021
10:00 AM PDT | 01:00 PM EDT
90 Minutes
Yuval Shapiro Instructor:
Yuval Shapiro
Webinar Id:

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$149 Live
$299 Corporate Live
$199 Recorded
$399 Corporate Recorded
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This webinar presents to the participants the new requirements of the standard and how they correlate with the regulatory changes in the EU.

Prior to engaging the process of establishing and certifying a QMS for medical devices or enhancing the QMS to the newly introduced requirements, a review of those requirements and how to approach them is important.

The webinar will present the evolution of the ISO13485 since its initial publication on 1988.

Also, the webinar will exhibit the last evolvement: Risk Approach and Regulatory Requirements Addressing.

In addition, timetables and several tips how to address the certification process will be introduced.

Why should you Attend:

  • The background for the revised ISO13485
  • The principles of ISO13485
  • ISO13485: 2016 sections
  • Main changes from the ISO13485: 2003

Areas Covered in the Session:
  • Provide a general overview of ISO13485: 2016
  • Examine new changes to the standard, especially Risk Approach
  • Discuss best practices for addressing the standard
  • Discuss best practices for implementation and potential pitfalls

Who Will Benefit:
  • Quality Managers
  • Quality Engineers
  • Engineering Managers
  • R&D Manager

Speaker Profile
Yuval Shapiro is the founder of QWV - Quality with Value, QA or RA Services. An expert for products and companies primarily related to medical devices that meet the real needs of their clientele. Substantial experience gained in various multi-discipline technology industries (Military, Telecom & Medical Devices), and give a high value contribution to quality and reliability projects related to the medical device and telecom industries.

More than 20 years of experience in QA; including MD and D RA and QA; QMS (21CFR - Part820, ISO13485, TL9000, CMDCAS, ISO9001). More than 20 years of experience in QA; including MD&D RA & QA; QMS (21CFR - Part820, ISO13485, TL9000, CMDCAS, ISO9001). EH and S Systems; QA or RA representative in R and D Projects. Risk Analysis as per ISO14791 & ISO31000. EMC & Safety Certifications.

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