help_outline Skip to main content
Add Me To Your Mailing List
Organization of Regulatory and Clinical Associates
Contact Information:
Organization of Regulatory and Clinical Associates
P.O. Box 3490
Redmond, WA 98073
HomeCurrent/Future Events Webinar - Introduction to the European Commission’s MDR Eudamed

Current/Future Events - Event View

This is the "Event Detail" view, showing all available information for this event. If the event has passed, click the "Event Report" button to read a report and view photos that were uploaded.

Webinar - Introduction to the European Commission’s MDR Eudamed

When:
Thursday, August 8, 2019, 8:00 AM until 8:45 AM
Where:
Webinar - link will be emailed to attendees 2 days prior to the meeting

Additional Info:
Category:
Webinar
Registration is closed
Payment In Full In Advance Only
Meetings and webinars are scheduled on Pacific Standard Time or Pacific Daylight Time, whichever applies.

Please make sure that the following email address is in your Safe Sender list: mailer@mail2.clubexpress.com. System messages like meeting announcements, registration confirmations, webinar login instructions as well as certificates of attendance are sent directly from this email address.

You will receive an email 2 days prior to the meeting date with the webinar login instructions or after payment is processed if registering closer to the meeting date. If you don't receive the instructions within this time frame, please contact us at info@orcanw.org as soon as possible.

PAID FEES ARE NON REFUNDABLE.

For webinar events, payment is REQUIRED at the time of registration.
Capacity:
100
No Fee
$60.00

The link to the webinar is intended for the registered person ONLY and should not be shared.
All attendees MUST be registered.

THIS IS A THURSDAY MEETING

The webinar will be presented by Eudamed.Eu (30 minute presentation, and 15 minute Q&A session)
Eudamed.eu was created to assist the MedTech industry with their MDR Eudamed knowledge, implementations, support, and the related Eudamed IT services and consulting. The CEO has brought invaluable knowledge to the company as a result of his technically managing the EC MDR Eudamed project.

Eudamed.eu provides the following:
1. MDR Eudamed IT training
2. Software as a Service for data processing and submission
3. Support services
4. Consultancy



https://eudamed.eu/index.php/about-us/


TOPIC:
MDR Eudamed Overview

TOPIC DESCRIPTION: This is a short introduction to MDR Eudamed where we will cover points such as registration, the current situation in regards to MDR and the timelines, IT project requirements, legacy devices (MDD certified devices) and the move away from the GMDN system. 

SPEAKER: Richard Houlihan – CEO - Eudamed.eu

SPEAKER BIOGRAPHY: Richard Houlihan was the technical manager for the European Commission overseeing the IT system MDR Eudamed from July 2017 until April 2019. His responsivities involved the design, development, and implementation of the MDR Eudamed application and the associated data exchange for machine-to-machine XML uploads.
Richard has been in IT related businesses for 25+ years, working with the European Commission for 8 years on Eudamed 2 and 3 (MDR Eudamed). He holds a BSc in Computing and a MBA Information management.

WHO: Clinical, regulatory, quality, manufacturing and legal

Attendance at this meeting may be applied as 1 point towards RAC re-certification.