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Practical: How to succeed in Software Validation for Medical Devices? 

Easy Medical Device
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Bill Stamm and Rafael Blanco from General Digital Software Services are helping us to have a better understanding of Software Validation. This topic is critical for Medical Device Manufacturers as the Healthcare world start to get digital.
More digital products that contain software, more software on the manufacturing side, more software to verify software. I mean, software is everywhere.
The new EU MDR is strengthening the requirements for Software and we need the experts to help. Bill and Rafael are specialized in this and they are the right SMEs to tell us exactly which mistake to avoid.
I will also ask them about artificial intelligence as this is a kind of software that is more complicated.
They also asked me to share with you some documents like the V-shape which describe the software validation process. Don’t hesitate to download it in the resource section.
About Bill Stamm
Mr. Stamm is the Vice President of Software Services at General Digital Corporation. He leads the Software Services team in sales and business management, growing global customer relations and partnerships, and oversees all software development, certification, IV&V testing, and documentation. Mr. Stamm joined General Digital in 2015. With over 25 years of experience in the field, his varied background has brought him from service and engineering into sales and marketing. Mr. Stamm has also owned several businesses and has worked as an international sales and marketing manager at various other technology companies, such as EMC and Practical Automation. Mr. Stamm holds degrees in Computer Engineering, as well as Business Administration and Management.
About Rafael Blanco
Mr. Blanco has extensive experience with Software Verification and Validation of Avionics systems and components. He has performed verification (integration testing, module testing, reviews) on Bleed Air Systems, Mechanical Actuators, Fuel Pumps, Fuel Tanks & Systems, Automatic Flight Control Systems, Engine Controls, Starters, Pneumatic Systems Equipment, Cooling Systems, Fly-by-Wire Systems, and Flight Management Systems. With over 25 years of experience in testing and project management, he has successfully brought his customers through FAA (Transport Canada, JAA) certifications for DO-178 projects both as a Verification Engineer and a Project Manager.
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Links from the Video
General Digital Software Services: gdsoftwareservi...
Bill Stamm Linkedin:
linkedin.com/in/bill-stamm-64118113
Rafael Blanco Linkedin:
linkedin.com/in/rafael-blanco-54963836
Document PDF to download: Link 1 and Link 2
Medtech prediction 2019: podcast.easyme...
FDA - General Principles of Software Validation: www.fda.gov/do...
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Social Media to follow
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Pinterest: / easymedicaldevice
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#engineering #medicaldevice #software

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9 сен 2024

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Комментарии : 11   
@EasyMedicalDevice
@EasyMedicalDevice 5 лет назад
Thanks to Bill Stamm and Rafael Blanco from General Digital Software Services for there good advice on how to succeed a Medical Device Software Validation. Don't forget to download their document on the show notes.
@tonygame9007
@tonygame9007 4 года назад
Thank you brother for setting this interview! This helps a lot❤👍🏻
@EasyMedicalDevice
@EasyMedicalDevice 4 года назад
You’re welcome
@akademiaiauditor6995
@akademiaiauditor6995 5 лет назад
Good interview Monir. Keep it up. Your energy is crazy :-)
@EasyMedicalDevice
@EasyMedicalDevice 5 лет назад
Akademia iAuditor thank you! Really appreciated. Let’s see if the energy increase on the next one lol.
@dhinakaranm4805
@dhinakaranm4805 5 лет назад
Hi, It is very useful to me. Requesting more videos related to software validation. i have a question that the medical device software contains many options but in a regular use we avail some of the options only. whether FDA requires the validation for all options which is given in the software or else we can validate the options what we are using regularly. Please give your reply.
@billstamm617
@billstamm617 5 лет назад
Dhinakaran, good question. All software must be validated. depending on the software and the risk it must not only have system level testing, but unit level testing. You cannot have unused code, or dead code present. So any code that is there must be tested. If you have code that is not being used, it should be removed. If your code is not written in a modular fashion where this is easy it could be difficult, time-consuming, and expensive. If you have any questions you can use the link on LinkedIn to contact me and we can discuss further. Thank you.
@madanjha8932
@madanjha8932 3 года назад
I want to do software validation of injection molding m/c. i am working in medical device company.
@TheRcj142
@TheRcj142 4 года назад
It was really useful interview for me to understand on medical devices V&V, could anyone help me out with some interview questions on this process which will led to us in depth knowledge on how to work in better ways in corporate sector while dealing with V&V
@JoJo-ll3de
@JoJo-ll3de 3 года назад
Tu es francophones je le sens
@EasyMedicalDevice
@EasyMedicalDevice 3 года назад
Lol, oui je suis francophone.
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