PLAY PODCASTS
Episode 5 – Medtech Prediction 2019

Episode 5 – Medtech Prediction 2019

2019 is here and as I read many media´s predictions for the medtech industry, I decided to also predicte myself what will be a trend. I will talk specifically about 2 axes which are Technologies and Regulations. Both are linked because as regulators we need to understand the technologies to be able to provide the right answer when we need to issue a regulation. The post Episode 5 – Medtech Prediction 2019 appeared first on Medical Device made Easy Podcast. Monir El Azzouzi

Medical Device made Easy Podcast

January 6, 2019

Audio is streamed directly from the publisher (archive.org) as published in their RSS feed. Play Podcasts does not host this file. Rights-holders can request removal through the copyright & takedown page.

Show Notes

The Year 2018 is over so let´s see what is ahead of the medical device industry in 2019. (Podcast episode page: https://podcast.easymedicaldevice.com/5/)

I will provide the audience with 2 axes of topics:

  • Technology trends
  • Regulatory changes

Some would say that these have nothing to do together but I disagree. As Medical Device Regulators, we need to understand technology to be accurate in our choices.

Is there any risk for the patient? What are the parameters you need to verify in a Technical File? You cannot do that without knowing what are the different technologies.

I will list you some technologies that you need to follow or to understand at least. As you may assume a lot of them will be digital or software based. So don´t think that this is the future because, in reality, it´s already here.

Regarding regulations, as there are new technologies, this should also change. We need to identify what is not accurate anymore on our regulations to cover these new technologies.

Recently, 2 documentaries were released “The bleeding edge” and “The implant files”. They focus on the fact that some regulations are not good enough. No regulation is really perfect it´s why some updates are needed. And I think the regulators understood that because a lot of countries are updating their laws. Europe with MDR and IVDR. The USA is now in the process to modernize the 510(k) process. MDSAP is helping to harmonize the regulations worldwide…

So many things are ongoing. Let me know if I forgot something. Write a comment below.

Resource

Podcast Episode 5 – Medtech Prediction 2019

Podcast Episode 5 – Medtech Prediction 2019

YouTube Video

https://youtu.be/ei-4gToN8Ek

Don’t forget to subscribe to the YouTube Channel for more videos. And activate the bell to get notified.

Channel Link: http://www.youtube.com/c/EasyMedicalDevice

The post Episode 5 – Medtech Prediction 2019 appeared first on Medical Device made Easy Podcast. Monir El Azzouzi

Topics

medicaldeviceregulationMEDTECHINDUSTRYregulatoryaffairsISO13485EUMDRMDR2017/745MedicalDeviceIndustryQualityManagementSystemFDAANVISATGAEURegulatoryComplianceAuditsNotifiedBodymeddevicetrainingcertificationbusinesstechnolo