FALLS CHURCH, Va. (PRWEB) March 12, 2020
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.
Read the full story at https://www.prweb.com/releases/fdanews_announces_eu_mdr_are_you_ready_part_ii_tips_for_assessing_your_readiness_prior_to_notified_body_review_webinar_mar_26_2020/prweb16937450.htm.
'/>"/>
| Source: PRWeb Copyright©2020 Vocus, Inc. All rights reserved |
Related medicine news :
1. FDAnews Announces — 1 Week Until EU-Medical Device Regulation Compliance Workshops March 17-20, 2020 - Philadelphia, PA
2. FDAnews Announces — 1 Week Until FDA Data Integrity: For Device and Pharma Firms, and Their Suppliers Workshop March 17-18, 2020, Philadelphia, PA
3. FDAnews Announces — Healthcare Innovation and FDA Regulation: Former FDA Commissioner Explains Growing Opportunities for Biomedical Products Webinar, Mar. 19, 2020
4. FDAnews Announces — Pharmacy Compounding Regulation: FDA’s Latest Guidance, Compliance & Enforcement Activities Webinar, Feb. 18, 2020
5. FDAnews/CenterWatch Announces — Real World Evidence and Data: A Tufts Study of 30 Pharma Companies Webinar January 23, 2020
6. FDAnews Announces — Postmarket Problems for Medical Devices: The Path to Resolution Workshop Feb. 19-20, 2020 - Atlanta, GA
7. FDAnews Announces — Understanding UDI in EU Device Regulations Webinar, Nov. 21, 2019
8. FDAnews Announces — 1 Week Until Conducting Advanced Root Cause Analysis and CAPA Investigations: Critical Thinking Skills and Innovative Techniques Nov. 13-14
9. FDAnews Announces — Early Bird Pricing Ends on Nov. 12, Building a World-Class Advertising and Promotion Review Program Dec. 10-11, 2019 Miami, FL
10. FDAnews Announces — Labeling for Prescription Drugs, Biologics and Combination Products:Complying with FDA’s Most Recent IFU Guidance Webinar, Oct. 29, 2019
11. FDAnews Announces — Medical Device Nonconforming Audit Findings: Corrective Action That’s Right for Your Company Webinar, Oct. 15, 2019
| Copyright © 2003-2012 Bio-Medicine. All rights reserved. ABOUT | CONTACT US | DISCLAIMER | PRIVACY POLICY | TERMS AND CONDITIONS |  |