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Medical Device News – March 2020 Review (EU MDR)

Medical Device News – March 2020 Review (EU MDR)

The month of March 2020 is over but there was a lot of information provided regarding the Medical Device industry so let's listen to the different news with Monir El Azzouzi The post Medical Device News – March 2020 Review (EU MDR) appeared first on Medical Device made Easy Podcast. Monir El Azzouzi

Medical Device made Easy Podcast

April 6, 2020

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Show Notes

In this episode of the Podcast, I will provide you with the situation for the month of march 2020 and what should happen next.

As you may know we are in the beginning of a pandemic and this is really a stressful situation for all countries worldwide. So this episode will also show you some elements that should be interesting for you to know during this period.

We will also discuss about the Notified Body Situation. There is a new Notified Body that was announced but this is not enough. We need more. Let’s see the numbers.

I will also list the MDCG guidances and regulatory updates that were released.

Finally, we will review what happened at Easy Medical Device during that month.

Don’t miss the links with all the source of information

Who is Monir El Azzouzi?

Monir El Azzouzi is a Medical Device Expert specialized in Quality and Regulatory Affairs.

After working for many years with big Healthcare company 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, Podcast, Online courses…

Links from the Video

Medical Device News March 2020 - Monir El Azzouzi - Medical Device made Easy Podcast - Easy Medical Device

The post Medical Device News – March 2020 Review (EU MDR) appeared first on Medical Device made Easy Podcast. Monir El Azzouzi

Topics

medicaldeviceregulationMEDTECHINDUSTRYregulatoryaffairsISO13485EUMDRMDR2017/745MedicalDeviceIndustryQualityManagementSystemFDAANVISATGAEURegulatoryComplianceAuditsNotifiedBodymeddevicetrainingcertificationbusinesstechnolo