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FDA’s Q-Submission Program for Medical Devices, Software-in-a-Medical Device Products & SaMD with Considerations for Using AI & ChatGPT
Overview: The U.S. Food and Drug Administration (FDA) has taken a major step toward modernizi..
Date : 22nd October 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
FDA Human Factors Usability Guidance | ISO 62366 & Draft Update Explained
Overview: Human Factors/Usability studies are essential in ensuring that medical devices are ..
Date : 29th May 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Minutes
How to Conduct an ACH Risk Assessment and Develop an Effective Risk Management Program
Overview: As a Financial Institution, a Third-Party Service Provider (TPSP) or a Third-Party ..
Date : 16th March 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Mandatory Paid Sick Leave vs Vacation vs PTO: What You Need to Know
Overview: Fifteen states and the District of Columbia now require employers to provide paid si..
Date : 22nd February 2022
Time : This Event is Over and the Recorded Copy is Available
Duration : 1 Hour 10 Mins