EU-MDR: Are You Ready?
Part II: Tips for Assessing Your Readiness Prior to Notified Body Review
An Exclusive Three-Part FDAnews Webinar Series

Friday, April 10, 2020 • 11:00 a.m. - 12:30 p.m. EDT


Note: This webinar has been rescheduled to April 10.

The new EU-MDR goes live in May 2020 to increase patient safety by making products more readily traceable.

You’ll need to make sure that the product information — including labeling content — is current on your website. And that the unique device identification for all your devices is uploaded to the European database on medical devices (EUDAMED).

Does your organization have the right strategies in place for a notified body review?

Join us for a webinar on April 10 for a discussion of the Plan-Do-Check-Act cycle where you’ll need to conduct internal audits for each EU-MDR element. In 90-minutes, medical device expert, Dan O’Leary will explain the relevant parts of Annex VII and how to integrate them into the internal audit program.

Webinar Takeaways:

  • Audit the Quality Management System (QMS) elements in Article 10
  • Review of the Annex II technical documentation supported by Annex I and Annex III
  • Understand the requirements for the Annex IX application
  • Recap the notified body document review in Annex VII
  • Understand the notified body audit based on Annex VII

Make sure you have the right strategies in place for regulatory compliance with the rigorous EU-MDR mandates! Join us by registering today for Part II or save 25% by registering for the complete three-part series.

The series also includes:

  • Part III: After May 2020, Ensuring Your Post-Market Surveillance Readiness via a Risk Management Framework
    Thursday, April 23, 2020, 1:30 p.m. - 3:00 p.m. EDT

Click here to register for the complete three-part series.

Part II Pricing



Webinar plus USB Audio Recording/Transcript
Learn more


add to cart

Webinar only
Learn more


add to cart

24/7 Encore plus USB Audio Recording/Transcript
Learn more


add to cart

24/7 Encore Presentation
Learn more


add to cart

USB Audio Recording/Transcript
Learn more


add to cart
Register for the
Three-Part Series


Who Will Benefit

  • Medical device / technology companies
  • Quality manager
  • Regulatory manager
  • Operations manager
  • Design manager
  • Technical manager
  • Clinical manager
  • Authorized representative in Europe


Meet Your Presenter

Dan O’Leary

Ombu Enterprises, LLC

Your webinar leader is Dan O’Leary, 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’ experience in quality, operations, and program management in regulated industries including aviation, defense, medical devices, and clinical labs. He has a master’s degree in Mathematics; is an ASQ certified Biomedical Auditor, Quality Auditor, Quality Engineer, Reliability Engineer, and Six Sigma Black Belt; and is certified by APICS in Resource Management.

MII logo

300 N. Washington St., Suite 200, Falls Church, VA 22046, USA

Phone 703.538.7600 | Fax 703.538.7676 | Toll free 888.838.5578 | Email

© 2020 FDAnews