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Overview: The
FDA 510(k) submission process remains one of the most crucial regulatory
pathwa..
Date : 29th October 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
10 Minutes excerpt from the recorded event for your review: Read the LinkedIn Article: Lin..
Date : 28th June 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Overview: In
the fast-evolving field of medical technology, ensuring the safety and efficacy
..
Date : 28th May 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Overview: FDA
has always prioritized the risk management of medical devices, adhering to its
..
Date : 27th February 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Overview: In
this informative webinar, we delve into the critical field of medical device
cyb..
Date : 20th June 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Overview: Testing
software to prove that it works and has no bugs is not sufficient to obtain ..
Date : 25th October 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
Overview: All life science
businesses are required to maintain their Quality Management System..
Date : 10th June 2021
Time : This Event is Over and the Recorded Copy is Available
Duration : 90 Mins
Overview: The
validation of computer systems (CSV) under FDA regulations has shaped the way
e..
Date : 25th November 2024
Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time
Duration : 90 Mins
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