![AI Act vs EU MDR 2017/745 are they compatible? [Erik Vollebregt]](https://cdn.podme.com/assets/podcast_img_placeholder_small.jpg)
AI Act vs EU MDR 2017/745 are they compatible? [Erik Vollebregt]
If you are working with Artifical Intelligence for your Medical Devices, then this episode is for you. We are alerting you about the new legislation that is planned for all Artificial Intelligence sof...
19 Heinä 20220s

Medtech Europe Forum interviews (MDR, EUDAMED, CER & MECOMED)
During my visit to the Medtech Europe Forum I had the chance to meet Fabien, Peter, Ronald, Inna and Rana. They shared with me some great information. Don't miss their interview. The post Medtech Euro...
12 Heinä 20220s

Medical Device News – July 2022 Regulatory Update
This podcast episode is the monthly review of the regulatory situation. Don't forget to download the document with all the links. The post Medical Device News – July 2022 Regulatory Update appeared fi...
5 Heinä 20220s

Attention! 1 year before UKCA is the law for Medical Devices in the UK
This is your last year to be compliant to UKCA otherwise Bye Bye the UK market. We tell you everything with Adam Rae on this episode. So listen carefuly and don't forget to download the cheat sheet. T...
28 Kesä 20220s
![Why is it great for Importers to be ISO 13485 certified? [Cristina Miroescu]](https://cdn.podme.com/assets/podcast_img_placeholder_small.jpg)
Why is it great for Importers to be ISO 13485 certified? [Cristina Miroescu]
We may think that ISO 13485 certification is only for Medical Device manufacturers but in this episode you will hear Cristina Miroescu from Sofmedica Group tell us why its company decided to be certif...
21 Kesä 20220s
![What are some Quality Common Mistakes? [Karandeep Badwal]](https://cdn.podme.com/assets/podcast_img_placeholder_small.jpg)
What are some Quality Common Mistakes? [Karandeep Badwal]
Karandeep Badwal will list us some of the common mistakes that he has always noticed. I will confirm some of them. If you are able to solve those you have made already 70% of the problems resolved. En...
14 Kesä 20220s

Medical Device News: June 2022 Regulatory Update
Medical device news June 2022 is focusing on IVDR 2017/746 date of applciation and consequences. Don't miss all the additional information on guidances, Training,,, The post Medical Device News: June ...
7 Kesä 20220s

Let’s introduce you to our eQMS SmartEye with Anindya Mookerjea
We have worked since more than a year on an eQMS called SmartEye and I have invited Anindya Mookerjea the CEO of SCube Technologies to present the tool and talk about the advantages of electronic Qual...
31 Touko 20220s



















