Upcoming Webinar
How to Manage the Legal Landmine of the FMLA, ADA and Workers Compensation in the Workplace!
Overview: Understanding how to navigate the Americans with Disabilities Act (ADA) is a legal n..
Date : 23rd September 2025
Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time
Duration : 90 Mins
Clinical Trial Systems: Trial Master File (TMF) and eTMF, & FDA’s Recent Draft Guidance for Electronic Records/Signatures Used in Clinical Trials
Overview: Organizations involved in the conduct of human clinical trials must meet rigorous re..
Date : 30th September 2025
Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time
Duration : 90 Mins
Charles H. Paul
510K Submission Process for Medical Devices
Overview: There are three types of 510(k) submissions that can be submitted – Traditional, Spec..
Date : 25th August 2023
Time : This Event is Over and the Recorded Content is Available
Duration : 75 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
Preventing Human Error in the Life Sciences - Pharmaceutical and Medical Device
Overview: Human Error occurs in all settings. In the world of pharmaceutical and medica..
Date : 29th July 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Preventing Medical Device Recalls – A Prevention Strategy
Overview: In a recent study, the FDA has reported a 95% increase in medical device recalls ..
Date : 28th June 2022
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Preparing for an FDA Audit? Learn the Best Behavior Practices and the Do’s and Don’ts
Overview: This webinar will begin by discussing and emphasizing the importance of truthfulness..
Date : 20th May 2022
Time : This Event is Over
Duration : 75 Mins