Medical Device made Easy Podcast

Medical Device made Easy Podcast

Listen Medical Device Regulation and Standards

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Avsnitt(413)

Grow your LinkedIn Profile with Karandeep Badwal

Grow your LinkedIn Profile with Karandeep Badwal

If you are looking to grow your LinkedIn profile then you should listen to this episode where Karandeep Badwal will give his learning being part of the LinkedIn Creator Accelerator Program. The post G...

27 Dec 20220s

Is EU MDR extended? with Erik Vollebregt

Is EU MDR extended? with Erik Vollebregt

I know you all heard about the extension of transition period for the EU MDR 2017/745. This is a good news, but let'S understand what this means and how you should interpret all this as there are some...

20 Dec 20220s

MDCG, Team-NB, BVMed & Team-PRRC tell you all about PRRC

MDCG, Team-NB, BVMed & Team-PRRC tell you all about PRRC

If you have a question about the role of a PRRC then most likely this will be answered by one of those expert. This podcast will display the Team-PRRC event where EU commission, Team-NB and BVMed answ...

13 Dec 20220s

Medical Device News – December 2022 Regulatory Update

Medical Device News – December 2022 Regulatory Update

All the latest regulatory news for the Medical Device Industry in 30 minutes The post Medical Device News – December 2022 Regulatory Update appeared first on Medical Device made Easy Podcast. Monir El...

6 Dec 20220s

How to choose the best Sterilization Method for Medical Devices?

How to choose the best Sterilization Method for Medical Devices?

This is a questions that I get asked when I am part of the design process of medical devices. Which Sterilization method should we choose? I invited Jane Scally to help us define the best practices wh...

29 Nov 20220s

Why Risk Management is important to Medical Device development?

Why Risk Management is important to Medical Device development?

Why is Risk Management so important? This is maybe something that a lot of regulators are asking you. "Do you have your Risk Management?" In this episode, we will explain to you why this is most criti...

22 Nov 20220s

Regulatory Pathway: How to reach the US market? [510k exempt]

Regulatory Pathway: How to reach the US market? [510k exempt]

If you are willing to reach out to the US there may be multiple strategies. We will talk today about MysteryVibe that started to evaluate the market and identified that their product is class IIa in E...

15 Nov 20220s

Your Software/IVD clinical report is completely WRONG!

Your Software/IVD clinical report is completely WRONG!

If you are in the Software and IVD industry we would bet that you are making your clinical data gathering wrong. Cesare Magri will explain to you why and how to correct that. So listen carefully to hi...

8 Nov 20220s

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