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Independent Contractor vs. Employee And the New Rules Issued by The Department of Labor

Independent Contractor vs. Employee And the New Rules Issued by The Department of Labor

Overview: For HR professionals, payroll leaders, managers, and business owners, worker classi..

Date : 29th April 2026

Time : This Event is Over and the Recorded Content is Available

Duration : 75 Mins

Supplier Selection and Contract Manufacturer Qualification Under FDA QMSR

Supplier Selection and Contract Manufacturer Qualification Under FDA QMSR

Overview: FDA’s QMSR places renewed emphasis on the way medical device companies evaluate, se..

Date : 24th March 2026

Time : This Event is Over and the Recorded Content is Available

Duration : 75 Mins

Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR in 2026

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

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

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

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

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

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

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

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

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

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

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)

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?

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

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