Since 2002 FX Conferences has been leading the way in producing distance learning and professional development opportunities for busy professionals. Our catalog is constantly growing and evolving to meet the needs and challenges facing those in the medical device, pharmaceutical, food & beverage and other industries. We team with industry-leading experts and content partners to offer timely and relevant presentations on a wide variety of topics. Browse our library, contact us if you have questions, and take control of your professional development!

Search By
Industry
Department

*Revisions to EN ISO 14971 and 13485 – What Do They Mean for Device Manufacturers?

In 2012, the European Union issued new versions of EN ISO 14971 on medical device risk management and EN ISO 13485 on quality management systems for devices. The two standards are now harmonized. You need to implement these major changes!


One source of confusion is the various versions of standards. This presentation explains the global system of standards, distinguishing between the international version, regional versions (such as the EU), and national versions (such as the UK, Canada, and the US). In addition, our speaker clarifies the role of harmonized standards and explains the EU’s regional version of the standards and their linkage to the directives.


The focus of the presentation is the impact of these changes on the Medical Device Directive. EN ISO 14971:2012 primarily affects the Essential Requirements, while EN ISO 13485:2012 deals with the conformity assessment paths. Our speaker explains the impact on both Annex I Essential Requirements and Annex II Full Quality Assurance System, and also addresses the content deviations in EN ISO 14971 which limit or restrict certain risk management practices.


This audio conference covers:


  • The impact of EN ISO 13485:2012 on the conformity assessment paths, especially MDD Annex II
  • The impact of EN ISO 14971:2012 on the Essential Requirements, MDD Annex I
  • The differences among international, regional, and country standards and how to distinguish them
  • The role of harmonized standards in the EU and how to determine when a standard becomes harmonized
  • How to get ready for the changes


About the speaker:


Dan O'Leary is President of Ombu Enterprises, LLC, a company offering training and execution in operational excellence, focused on analytic skills and a systems approach to operations management. Dan has more than 30 years of experience in quality, operations, and program management in regulated industries including aviation, defense, medical devices, and clinical labs. He has a Masters Degree in Mathematics and is an ASQ-certified Biomedical Auditor, Quality Auditor, Quality Engineer, Reliability Engineer, and Six Sigma Black Belt. He ia also certified by APICS in Resource Management.


Who should attend?


  • Any company with a CE Mark to the MDD, AIMD, or IVDD
  • Regulatory Affairs Managers
  • Risk Management professionals
  • Quality Managers
  • Quality Engineers


Available Dates:


  • Tuesday, December 4th, 2012 - 3:30pm Eastern
  • Wednesday, December 5th, 2012 - 9:30am Eastern
  • Thursday, December 6th, 2012 - 2:00pm Eastern
  • Friday, December 7th, 2012 - 10:00am Eastern


*Please select the date you would like to attend from the dropdown menu below.


Product Details

Dan O'Leary, Ombu Enterprises
*Revisions to EN ISO 14971 and 13485 – What Do They Mean for Device Manufacturers?
Title: President
Duration: 60 minutes
Event Type: Previously recorded on 2012-11-14
Item #: ac20121114R
7 Dec 2012 
Registration Price:
$249.00

Order Info

Select Order Type:  
Include Transcript With Order?:  
Select Conference Date:  
Convert to my time zone.
Quantity
More
Less
 
 
Product Rating:

Reviews for *Revisions to EN ISO 14971 and 13485 – What Do They Mean for Device Manufacturers?

Be the first to submit a review on this event!
Review this Conference
© Copyright 2014
FX Conferences.
All rights reserved.

FAQ  |  Medical Translation  |  Search  |  Privacy  |  Terms of Use  |  Contact