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Project Management for CSV in FDA-Regulated Environments (CSA, GAMP®5 2nd Ed.) — with a Brief AI/ChatGPT Overview for PM Support
Overview: Computer System Validation (CSV) has underpinned FDA compliance in regulated industr..
Date : 30th October 2025
Time : This Event is Over and the Recorded Content is Available
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Clinical Trial Systems: Trial Master File (TMF) and eTMF, & FDA’s Recent Draft Guidance for Electronic Records/Signatures Used in Clinical Trials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 : 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
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
How To Conduct Effective Workplace Investigations That Will Meet Compliance Guidelines and Regulations
Overview: For HR professionals and those responsible for employee relations, conducting workp..
Date : March 13, 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
I-9 Audits & ICE Workplace Raids: What Employers Must Do to Stay Compliant
At Amorit Education, we recently hosted a 90-minute expert-led webinar featuring Margie Faulk, a com..
Date : February 26, 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Nacha Updates in the ACH Network (Operations Bulletins – RFC and RFI Details)
Overview: The ACH Network continues to evolve, driven by technological advancements, regulato..
Date : February 26, 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
What is in Store for Employers When Updating Employee Handbooks in 2025?
Overview: Imagine this: Your employee handbook, a tool designed to guide and protect your org..
Date : 17th January 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
THE DOL’s New Rule on Independent Contractors
Overview: Misclassifying workers as either independent contractors or employees carries signif..
Date : 16th January 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
Functional and System Requirements for Systems Regulated by FDA in 2024
Overview: The validation of computer systems (CSV) under FDA regulations has shaped the way e..
Date : 25th November 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Detecting Truth, Deception and Lies when Conducting an Workplace Investigation
Overview: Workplace investigations are often associated with cases of harassment, discriminati..
Date : 20th November 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Medical Device Hazard analysis following ISO 14971 - Understanding The Process in Detail in 2024
Overview: In the world of medical device development, the US FDA places a high priority on ri..
Date : 14th August 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
Mastering Mobile App & Medical Device Software Validation and Cybersecurity in FDA-Regulated Environments
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
Human Factors/ Usability Studies following ISO 62366 , the FDA Guidance and the new FDA Draft Guidance
Overview: Human Factors/Usability studies are essential in ensuring that medical devices are ..
Date : 25th June 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
Best Practices for Auditing a Vendor of Computer Systems Regulated by FDA
10 Minutes excerpt from the recorded event for your review:Read the LinkedIn Article: LinkedIn ..
Date : 30th May 2024
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins