ISO13485: 2016 - Quality Management Systems for Medical Devices

Posted By : User Ref No: WURUR49487 0
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  • TypeWebinar
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  • Location Fremont, California, United States
  • Price
  • Date 13-02-2020
ISO13485: 2016 - Quality Management Systems for Medical Devices, Fremont, California, United States
Webinar Title
ISO13485: 2016 - Quality Management Systems for Medical Devices
Event Type
Webinar
Webinar Date
13-02-2020
Last Date for Applying
13-02-2020
Location
Fremont, California, United States
Organization Name / Organize By
Compliance4all
Organizing/Related Departments
Online Training
Organization Type
Organization/Company
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Business Development

Administration/Management

Advertising/Marketing

Medical/Healthcare/Hospital

Location
Fremont, California, United States

Overview:

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 you should 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.

Event link:

https://www.compliance4all.com/webinar/--502888LIVE?channel=eventsget_2020_SEO

Contact Info

Netzealous LLC,DBA -Compliance4all

Email: [email protected]

Phone: +1-800-447-9407

Website: https://www.compliance4all.com/

Others Details

Contact Info Netzealous LLC,DBA -Compliance4all Email: [email protected] Phone: +1-800-447-9407 Website: https://www.compliance4all.com/

Registration Fees
Available
Registration Fees Details
$150 Live $290 Corporate Live $190 Recorded $390 Corporate Recorded
Registration Ways
Website
Address/Venue
  Online  Pin/Zip Code : 94539
Landmark
California
Official Email ID
Contact
Netzealous LLC,DBA -Compliance4all

Contact Info Netzealous LLC,DBA -Compliance4all Email: [email protected] Phone: +1-800-447-9407 Website: https://www.compliance4all.com/

[email protected]

   8004479407    Fax No: 94539