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Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR in 2026
Overview: In 2026, data integrity and privacy risks don’t sit in one department—they show up ..
Date : 19th March 2026
Time : This Event is Over
Duration : 90 Mins
Employers Should Prepare for Immigration Raids in 2026! This Means More I-9 Audits for Employers by ICE
Overview: Worksite immigration enforcement can turn into an operational crisis faster than mos..
Date : 26th February 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
2026 Nacha Rules Changes (Part 1): Fraud Monitoring & Ops Bulletins
Overview: The ACH Network runs on precision—formats, timing, authorizations, monitoring expec..
Date : January 28, 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 120 Mins
Risk-Based Excel Spreadsheet Validation and FDA Compliance - Risk-Based CSV/CSA & Part 11
Overview:FDA inspections and audits continue to put a bright spotlight on data integrity—especiall..
Date : 27th January 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
FDA’s QMSR is Coming: Practical Readiness for Quality Teams
Overview: With the FDA’s Quality Management System Regulation (QMSR) taking effect in February..
Date : 21st January 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
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Clinical Trial Systems: Trial Master File (TMF) and eTMF, & FDA’s Recent Draft Guidance for Electronic Records/Signatures Used in Clinical Trials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