Regulation (EU) 2017/745 (MDR)
Jul 22, 2024 ·
6m 57s
Download and listen anywhere
Download your favorite episodes and enjoy them, wherever you are! Sign up or log in now to access offline listening.
Description
Welcome to the new Di Renzo Regulatory Affairs podcast!In the ever-evolving landscape of medical device regulation, it is crucial to stay up-to-date. That's why today we'll delve into Regulation (EU)...
show more
Welcome to the new Di Renzo Regulatory Affairs podcast!In the ever-evolving landscape of medical device regulation, it is crucial to stay up-to-date. That's why today we'll delve into Regulation (EU) 2023/607, a significant amendment to Regulation (EU) 2017/745 (MDR) that introduces an extension of the transition period and defines the criteria for benefiting from it.As Regulatory Affairs experts dedicated to Class I medical devices, Di Renzo Regulatory Affairs is ready to support manufacturers in this delicate transition process.In this podcast, we will guide you through the details of Regulation 2023/607, clarifying:
show less
- Which Class I medical devices are eligible for the extension
- How to correctly assess the classification of your device
- What are the specific timelines for the extension
- How to make the most of this additional period to prepare for the MDR
- Introduce Di Renzo Regulatory Affairs and its expertise in medical device regulation.
- Highlight the importance of the MDR and its impact on Class I medical device manufacturers.
- Emphasize the value of Di Renzo Regulatory Affairs' services in helping manufacturers comply with the MDR.
- Encourage listeners to subscribe to the podcast and leave reviews.
Information
Author | Di Renzo Regulatory Affairs |
Organization | Di Renzo |
Website | - |
Tags |
Copyright 2024 - Spreaker Inc. an iHeartMedia Company