FDAnews Announces -- EU-MDR: Are You Ready? Part II: Tips for Assessing Your Readiness Prior to Notified Body Review Webinar, Mar. 26, 2020

Be prepared for the notified body review under the new EU-MDR. Join us on March 26 for compliance strategies to meet EU-MDR mandates.

News provided by

FDAnews

Mar 12, 2020, 00:00 ET

FALLS CHURCH, Va., March 12, 2020 /PRNewswire-PRWeb/ -- EU-MDR: Are You Ready?
An Exclusive Three-Part FDAnews Webinar Series
Part II: Tips for Assessing Your Readiness Prior to Notified Body Review
Thursday, March 26, 2020 • 1:30 p.m.-3:00 p.m. EDT
https://www.fdanews.com/part2eumdr

Get ready for EU-MDR's deadline in May.

How current is the product labeling on one's website? Is your unique device identification (UDI) uploaded to the European database on medical devices (EUDAMED)?

The new EU-MDR is designed to increase safety by making products more readily traceable and one will need to have the right strategies in place.

Join us for a webinar on March 26 for assessing attendees readiness prior to a notified body review:

  • Implement strategies to review technical documentation to ensure regulatory requirements and the general safety and performance requirements (GSPR) are addressed
  • Understand how a product review is undertaken by a notified body
  • Learn how to insert a new symbol on the label on instructions use (IFUs) that are being published — for the first time — in electronic rather than in paper form
  • Discover what additional symbols must be included relating to device reprocessing and safety
  • Find out what specific details of the organization's EC representatives' symbol, name, and address must be provided on the label

Make sure the right strategies are in place for regulatory compliance with the rigorous EU-MDR mandates!

This webinar is part two of a three-part online series on EU-MDR readiness. Save 25% by registering for the complete three-part series:

  • 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

  • Part I: The Real Role of the Person Responsible for Regulatory Readiness & Compliance

Purchase as an Encore Presentation. Recorded on Thursday, Feb. 20, 2020

Interested in registering multiple sites?
Call 888.838.5578 in the U.S. or +1 703.538.7600 globally to learn about our special multisite discount.

Webinar Details:
EU-MDR: Are You Ready?
An Exclusive Three-Part FDAnews Webinar Series
Part II: Tips for Assessing Your Readiness Prior to Notified Body Review
Thursday, March 26, 2020 • 1:30 p.m.-3:00 p.m. EDT
https://www.fdanews.com/part2eumdr

Tuition:
$287 per site

Easy Ways to Register:
Online: https://www.fdanews.com/part2eumdr?hittrk=20312VOCUS
By phone: 888.838.5578 or 703.538.7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.

SOURCE FDAnews

Related Links

https://www.fdanews.com/