Medical Device made Easy Podcast

Medical Device made Easy Podcast

Listen Medical Device Regulation and Standards

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Jaksot(414)

Medical Device News: December 2021 Regulatory Update

Medical Device News: December 2021 Regulatory Update

Here is the last Medical Device News for this year, I will cover all the updates that happen in the EU, UK, Switzerland,, US and Saudi Arabia. We will also review the situation for Notified Bodies. I ...

7 Joulu 20210s

Let’s unleash “MDR Classification surprises” [MDR 2017/745]

Let’s unleash “MDR Classification surprises” [MDR 2017/745]

The MDR classification was hidding some surprises and I have asked Frank Matzek from Biotronik to tell us more about the products and rules we need to take care of. So Enjoy! The post Let’s unleash “M...

30 Marras 20210s

How to approach your Notified Bodies? [Dr. Royth von Hahn – TÜV SÜD]

How to approach your Notified Bodies? [Dr. Royth von Hahn – TÜV SÜD]

Really great discussion with Dr Royth von Hahn from TÜV SÜD. He is providing some solutions on how to talk to your Notified Body. This would help Medical Device manufacturers. The post How to approach...

23 Marras 20210s

Is it possible to Private Label a Medical Device under MDR & IVDR?

Is it possible to Private Label a Medical Device under MDR & IVDR?

OEM OBL is really used a lot by Medical Device Manufacturers. But this is not possible anymore with EU MDR. So please listen to that as maybe you are doing it without knowing. The post Is it possible ...

16 Marras 20210s

How to improve your QA RA Communication with Lesley Worthington?

How to improve your QA RA Communication with Lesley Worthington?

Lesley Worthington is a career coach and will help you understand why improving your communication skills within QA RA can be a booster for you. We will talk about our experience as she also worked in...

9 Marras 20210s

Medical Device News – November 2021 latest update

Medical Device News – November 2021 latest update

Latest update will focus on IVDR proposal, Artificial intelligence, Notified Bodies situation and MDCG guidances. Other elements will also be discussed. I hope you'll enjoy! The post Medical Device Ne...

2 Marras 20210s

How does the EU Commission plan to save IVDR 2017/746?

How does the EU Commission plan to save IVDR 2017/746?

BREAKING NEWS: The EU Commission issued a proposal to delay some IVDR date of application but it is not a complete postponment so don't use this word. Listen the interpretation of Erik Vollebregt on t...

26 Loka 20210s

How to comply with MDR when products contain CMR Substances?

How to comply with MDR when products contain CMR Substances?

Ana Luiza is my guest and we will explain to you how to be sure that your are compliant with CMR substances on your product. CMR will be reviewed during an audit and apparently there were a lot of mis...

19 Loka 20210s

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