https://www.youtube.com/embed/B4AbITzsGqI?version=3&rel=1&showsearch=0&showinfo=1&iv_load_policy=1&fs=1&hl=en-US&autohide=2&wmode=transparent

Recently EUDAMED made a major Update which was the release of the Device registration module. This is something that all Medical Device manufacturers need to listen to as this may impact their workload.

Richard Houlihan from Eudamed.com accepted to come and tell us more about this update and provide you also with some advice on how to manage it.

So we will talk:

• EUDAMED progress

Richard Houlihan is also providing training to your team on how to implement EUDAMED so don’t miss it. The links are below.

Richard Houlihan has been in IT-related businesses for 25+ years. He holds a BSc in Computing and an MBA in Information management. The varying IT roles have led to him living in several countries, working across 6 blue chips, 3 start-ups, and 3 different directorates within the European Commission.

Monir El Azzouzi is a Medical Device Expert specialized in Quality and Regulatory Affairs. After working for many years with big Healthcare companies and particularly Johnson and Johnson, he decided to create EasyMedicalDevice.com to help people have a better understanding of the Medical Device Regulations all over the world. He now created the consulting firm Easy Medical Device GmbH and developed many ways to deliver knowledge through Videos, podcasts, Online courses…

• Richard Houlihan Linkedin Profile: https://www.linkedin.com/in/richard-houlihan/

Training sessions

• Training: 26th & 27th October https://eudamed.com/index.php/product/live-online-eudamed-training-26th-27th-october-2021/

For the manufacturers, without too many UDI DI’s an offer that includes our templates.

• Up to 100 UDI DI’s https://eudamed.com/index.php/product/eudamed-saas-100/

The post EUDAMED Update: Should you register your medical devices now? appeared first on Medical Device made Easy Podcast. Monir El Azzouzi