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Medical Device Cybersecurity Following FDA’s 2026 Premarket Guidance
Overview Cybersecurity is now a central part of FDA’s review expectations for many connected, ..
Date : 28th May 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
FDA Guidance for Use of Social Media by Regulated Industries
Overview: In the early days of social media, regulatory agencies were observers — watching as..
Date : 30th April 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Effective Technical Writing for Medical Devices: Improving Your Skills for Clear and Concise Communication
Overview: In the world of medical device manufacturing, technical writing is more than just a..
Date : 27th March 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
510K Submission Process for Medical Devices
Level:- Beginner to Intermediate Overview: There are three types of 510(k) submissions t..
Date : 21st November 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
FDA Human Factors for Medical Devices: Navigating the New Category 1, 2 & 3 Framework
OverviewFDA's 2026 Human Factors guidance has changed the way medical device manufacturers determin..
Date : 28th September 2026
Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time
Duration : 90 Mins