Тёмный

Understand IEC 62304 for Software Medical Devices with Adnan Ashfaq 

Easy Medical Device
Подписаться 13 тыс.
Просмотров 7 тыс.
50% 1

► Webpage: podcast.easymedicaldevice.com...
If you are developing Medical Device software then IEC 62304 is an important standard for you. In this episode, Monir El Azzouzi invited Adnan Ashfaq from Pharmi Med Ltd to explain to us what is this standard.
He will also mention some key links to the EU MDR 2017/745 and to other standards. Here are some of the questions asked:
- Which medical device companies should use IEC 62304
- Do I need to be a Software developer to be able to work on IEC 62304?
- What is the difference between software classification provided by IEC 62304 and EU MDR 2017/745.
Adnan is offering also a document to download which will help you during your projects with this standard.
-----------------------------------------------------------------------------------------------------------------------------
► Who is Adnan Ashfaq?
Adnan Ashfaq is a Quality, Regulatory & Validation Specialist with almost 20 years of experience in Medical Device, Biotech, and Pharmaceutical industries.
Adnan founded Pharmi Med in 2011 and has since been supporting Medical device companies around the labyrinth of regulations and assisting them in flying through successful audits.
He has been working with start-up companies and multinationals in developing new products since 1999. With regulations tightening up, especially in Europe, Pharmi Med is enabling and trying to help simplify the compliance conundrum to ensure manufacturers reach their desired market and stay in the market.
-----------------------------------------------------------------------------------------------------------------------------
► Who is Monir El Azzouzi?
Monir El Azzouzi is a Medical Device Expert specialized in Quality and Regulatory Affairs.
After working for many years with big Healthcare company and particularly Johnson and Johnson, he decided to create EasyMedicalDevice.com to help people have a better understanding of the Medical Device Regulations all over the world.
He now created the consulting firm Easy Medical Device GmbH and developed many ways to deliver knowledge through Videos, Podcast, Online courses...
--------------------------------------------------------------------------------------------
► Links from the Video
■ Adnan Ashfaq Linkedin: / adnan-ashfaq-44478121
■ Pharmi-Med Ltd: www.pharmi-med.com/
■ SaMD audit template: mailchi.mp/easymedicaldevice/...
■ MDCG 2019-11: ec.europa.eu/docsroom/documen...
■ IMDRF guidance on SaMD: www.imdrf.org/workitems/wi-sam...
■ IEC 62304 standard (affiliate): tidd.ly/2Bfjz4a
■ Episode 81- Process Validation with Adnan Ashfaq: podcast.easymedicaldevice.com...
-------------------------------------------------------------------------------------------
► Social Media to follow
■ Monir El Azzouzi Linkedin: / melazzouzi
■ Twitter: / elazzouzim
■ Pinterest: / easymedicaldevice
■ Instagram: / easymedicaldevice
------------------------------------------------------------------------------------------
#easymedicaldevice #medicaldevices #Regulatorycompliance

Опубликовано:

 

8 авг 2024

Поделиться:

Ссылка:

Скачать:

Готовим ссылку...

Добавить в:

Мой плейлист
Посмотреть позже
Комментарии : 18   
@mooudamirkavei6007
@mooudamirkavei6007 8 месяцев назад
Thanks so much Monir and Adnan for very informative video. Hope to see more and more videos on SaMD.
@vishwasnagaraju8260
@vishwasnagaraju8260 9 месяцев назад
Very well spoken Adnan.
@jonathanphillips5514
@jonathanphillips5514 2 года назад
Excellent video in what is confusing area! Thanks
@va222an
@va222an 3 года назад
Hi All, What kind of software procedures you follow in Verification and validation testing? Like do we do blackbox testing, Regression testing? Any inputs on test plan?
@vishnudas7839
@vishnudas7839 3 года назад
Really informative Monir.
@daithideburca98
@daithideburca98 4 года назад
Very informative, would love to see how equivalence is going to be addressed in Software, how would you compare two pieces of samd one approved v a new application
@EasyMedicalDevice
@EasyMedicalDevice 4 года назад
I think this is a challenging topic. You should define some criteria that are comparable but will this be enough. I will investigate.
@priyankap4433
@priyankap4433 4 года назад
It was very informative Monir. Please clarify :Do I have to a have a Dedicated QMS(using 13485 or 21CFR 820) for Software as a medical device (SaMed). Thank you Regards Priyanka
@EasyMedicalDevice
@EasyMedicalDevice 4 года назад
Yes you need one. For class I no need to be certified but for other classes it should be certified by a notified body
@priyankap4433
@priyankap4433 4 года назад
@@EasyMedicalDevice Many thanks Monir.
@navdeepgill9729
@navdeepgill9729 4 года назад
Very informative and good coverage, Only One place where i could not follow was @10:10 , There are 4 critical documents required for the IEC62304 ? Please add some more information around that. One i could understand was clinical Management and Risk Management, Can you please explain others aswell.
@adnanashfaq9163
@adnanashfaq9163 4 года назад
The documents are IMDRF - n41 SaMD clinical Evaluation IMDRF - n23 SaMD QMS IMDRF - n10 SaMD Key Definitions IMDRF - n12 SaMD Risk Categorisation
@navdeepgill9729
@navdeepgill9729 4 года назад
@@adnanashfaq9163 Thanks for the quick response.
@josejimeneza5816
@josejimeneza5816 Год назад
This video is Gold
@EasyMedicalDevice
@EasyMedicalDevice Год назад
Thanks for your support 🙏
@pranav203
@pranav203 2 года назад
I want to sincerely thank you for the very informative video. I’ve been in the medical device quality engineering space and this information is very useful. 👍🏼
@EasyMedicalDevice
@EasyMedicalDevice 2 года назад
You‘re welcome
Далее
IEC 60601 explained by Leo Eisner (Medical Devices)
31:10
SCHOOLBOY. Последняя часть🤓
00:15
Просмотров 948 тыс.
A Quick Look At Linux Mint 22 "Wilma"
20:14
Просмотров 2,8 тыс.
Risk control measures in medical device software
14:56
Просмотров 4,1 тыс.