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.