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Medical Device Hazard Analysis Under FDA QMSR: A Practical ISO 14971 Guide
OverviewHazard analysis has always played an important role in medical device safety. Under FDA’s ..
Date : 25th August 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
Nacha Rule – Third-Party Sender (TPS) Roles and Responsibilities - What to Know
Overview: In 2022, Nacha implemented significant updates to its Operating Rules to enhance cl..
Date : 20th March 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
How to Conduct an ACH Risk Assessment and Develop an Effective Risk Management Program
Overview:In today's digital payment landscape, Financial Institutions, Third-Party Service Provide..
Date : 22nd February 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
FDA Biocompatibility in 2026: What to Test, What to Justify, and What to Submit
Overview A medical device can undergo extensive biocompatibility testing and still encounter ..
Date : 16th November 2026
Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time
Duration : 120 Mins