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How to evaluate your Medical Devices in 3 Steps with Heikki Pitkänen?

How to evaluate your Medical Devices in 3 Steps with Heikki Pitkänen?

If you have a product and you want to evaluate if this is a Medical Device, then you need to follow the 3 steps that we will discuss on this episode. Heikki Pitkänen's platform is providing a solution for your to evaluate your device and he offers it for free to the listeners of this podcast. Thanks to him. The post How to evaluate your Medical Devices in 3 Steps with Heikki Pitkänen? appeared first on Medical Device made Easy Podcast. Monir El Azzouzi

Medical Device made Easy Podcast

December 2, 2019

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Show Notes

This week we’ll start back with the basic steps to follow to evaluate your Medical Devices. It will seem basic for some people but you should not be so sure.

The new EU MDR 2017/745 is coming with many surprises and one of them is the fact that some products without a Medical purpose will now be considered as a Medical Device. So what you think is now changing.

With Heikki Pitkänen, we will explore 3 steps with you to evaluate your Medical Devices. It’S clearly mandatory for you to go through them.

  • Step 1: Qualification of your Medical Device
  • Step 2: Classification of your Medical Device
  • Step 3: Best route to assess your Medical Device

After you followed those 3 steps, you are nearly sure to have a project built on a clear foundation.

In this episode, Heikki offers you access to his platform so you can evaluate your Medical Device and learn more about it. Don’t forget to download the giveaway which includes the promo code.

Who is Heikki Pitkänen?

Heikki is the CEO and founder of Lean Entries Ltd., a group of regulatory experts in the area of global medical device regulations providing unique digital regulatory services as well as traditional consulting for the MedTech sector from academies and startups to multinational enterprises.

Heikki has two decades of experience from medical device development, certification, accredited testing and standardization, most lately as the Notified Body site manager at SGS. He is a member of the CEN-CENELEC Advisory Board for Healthcare Standards.

Links

Heikki Pitkänene on the Medical Device made Easy Podcast about the evaluation of Medical Devices with EU MDR 2017/745

The post How to evaluate your Medical Devices in 3 Steps with Heikki Pitkänen? appeared first on Medical Device made Easy Podcast. Monir El Azzouzi

Topics

medicaldeviceregulationMEDTECHINDUSTRYregulatoryaffairsISO13485EUMDRMDR2017/745MedicalDeviceIndustryQualityManagementSystemFDAANVISATGAEURegulatoryComplianceAuditsNotifiedBodymeddevicetrainingcertificationbusinesstechnolo