Recorded Webinars

Explore a wealth of knowledge at your own pace with Amorit Education's recorded webinars. Click to access an extensive library of recent and past sessions across diverse industries. Make a purchase and receive the download link via email almost instantaneously, allowing you to dive into expert-led content whenever, wherever suits you best.



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

THE DOL’s New Rule on Independent Contractors

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

Effective Succession Planning for Today’s Challenges

Effective Succession Planning for Today’s Challenges

Overview: Succession planning has become a critical priority in 2024 as organizations face un..

Date : 15th January 2025

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

Duration : 90 Mins

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligence (AI) and Machine Learning (ML)-

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligence (AI) and Machine Learning (ML)-

Overview: As the life sciences industry, encompassing pharmaceuticals, medical devices, biotech..

Date : 13th January 2025

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

Duration : 90 Mins + Q&A

Functional and System Requirements for Systems Regulated by FDA in 2024

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

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

Excel Spreadsheet in FDA Regulated Environment - Ensuring Data Integrity and 21 CFR Part 11 Compliance

Excel Spreadsheet in FDA Regulated Environment - Ensuring Data Integrity and 21 CFR Part 11 Compliance

Overview:The use of Excel in FDA-regulated environments extends beyond basic data organization and a..

Date : 19th November 2024

Time : This Event is Over

Duration : 75 Mins

2024 I-9 Form Update: Essential Changes and Audit Compliance

2024 I-9 Form Update: Essential Changes and Audit Compliance

Overview: The recent updates to the Form I-9 and Employment Authorization Document (EAD) guide..

Date : 12th November 2024

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

Duration : 90 Mins

Multi-State employment - Manage Payroll for Remote & Distributed Teams

Multi-State employment - Manage Payroll for Remote & Distributed Teams

Overview: Navigating the complexities of multistate payroll tax compliance has always been a ..

Date : 04th November 2024

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

Duration : 90 Mins

Navigating the New DOL Rule: Independent Contractor vs Employee Classification

Navigating the New DOL Rule: Independent Contractor vs Employee Classification

Overview: The U.S. Department of Labor (DOL) has recently issued a new final rule, effective ..

Date : 31st October 2024

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

Duration : 75 Mins

Business Process Mapping – How to Prepare a Detailed System & Data Roadmap for a Clinical Trial Regulated by FDA

Business Process Mapping – How to Prepare a Detailed System & Data Roadmap for a Clinical Trial Regulated by FDA

Overview: Conducting human clinical trials requires strict adherence to government regulatory ..

Date : 30th October, 2024

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

Duration : 90 Mins

Preparing a FDA 510(k) submission - What to Know in 2024

Preparing a FDA 510(k) submission - What to Know in 2024

Overview: The FDA 510(k) submission process remains one of the most crucial regulatory pathwa..

Date : 29th October 2024

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

Duration : 60 Mins

Scrutinizing Test Method Validation (TMV) to Verify the Performance of a Medical Device

Scrutinizing Test Method Validation (TMV) to Verify the Performance of a Medical Device

Overview: Test Method Validation (TMV) is a critical yet often misunderstood requirement in t..

Date : 21st October 2024

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

Duration : 90 Mins

Protect Your Workplace: Comply with the EEOC's New Harassment Guidance

Protect Your Workplace: Comply with the EEOC's New Harassment Guidance

10 Minutes excerpt from the recorded event for your review: Read the LinkedIn Article: Lin..

Date : 11th September 2024

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

Duration : 90 Mins

Best Practices for Responding to a Form 483 Citation and/or Warning Letter Issued by FDA in 2024

Best Practices for Responding to a Form 483 Citation and/or Warning Letter Issued by FDA in 2024

Overview: The U.S. Food and Drug Administration (FDA) plays a critical role in safeguarding p..

Date : 30th August 2024

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

Duration : 90 Mins

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