Medical Device made Easy Podcast

Medical Device made Easy Podcast

Listen Medical Device Regulation and Standards

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Avsnitt(413)

Hire your QA RA person with no Budget 

Hire your QA RA person with no Budget 

We feel your pain when your bosses ask you to hire a QA RA person, but the challenge is that there is no Budget for it. But you want to impress them, so what to do. In this episode Mitch Robbins a pro...

8 Aug 20230s

Who should be on your Risk Management Dream Team?  

Who should be on your Risk Management Dream Team?  

Everyone is talking about Risk Management file and ask you to provide that to them. But should you do that alone or identify the best partners on your team to be successful. This is what Naveen Agarwa...

1 Aug 20230s

Artificial Intelligence in the Medical Device Industry

Artificial Intelligence in the Medical Device Industry

There is still this misunderstanding about AI, and we wanted to discuss about AI for Medical Devices to really understand what this is. I have invited Christophe Girardey from Wega to put some light i...

25 Juli 20230s

Validation of Quality Software in Medical Devices 

Validation of Quality Software in Medical Devices 

Software validation when used on patient is common and mandatory. But now when we tell you that you should validate also the software you are using to record your documents, CAPAs, or work on the elem...

18 Juli 20230s

How to register Medical Devices in Saudi Arabia?

How to register Medical Devices in Saudi Arabia?

Saudi Arabia is a major actor in the Medical Device world. A lot of companies are willing to enter this market that can help them to reach also other regions of the Middle East. We will discuss with A...

11 Juli 20230s

Medical Device News – July 2023 Regulatory Update

Medical Device News – July 2023 Regulatory Update

july 2023regulatory update The post Medical Device News – July 2023 Regulatory Update appeared first on Medical Device made Easy Podcast. hamza benafqir

4 Juli 20230s

What should you know on UKCA extension

What should you know on UKCA extension

UK decided to add more time to implement the UKCA. Apparently, the EU amendment to extend the EU MDR and IVDR was also something they looked at to define their timeline. So, let’s see what will this m...

27 Juni 20230s

How to connect Software dev and QA RA Team  

How to connect Software dev and QA RA Team  

You may be on the business of Software development and you ask yourself why your Dev team is not really happy to work with Quality and Regulatory affairs team? In this episode, we will discuss with Ch...

20 Juni 20230s

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