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.



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

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

Overview: On April 29, 2024, the Equal Employment Opportunity Commission (EEOC) issued its fi..

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

Mandatory Paid Sick Leave in 2024 - Breaking Through the Quagmire and Quandary of Compliance

Mandatory Paid Sick Leave in 2024 - Breaking Through the Quagmire and Quandary of Compliance

Overview: As of 2024, eighteen states plus the District of Columbia have mandated that employer..

Date : 28th August 2024

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

Duration : 75 Mins

An Advanced Course on Lean Documents, Lean Configuration, and Document Control in 2024

An Advanced Course on Lean Documents, Lean Configuration, and Document Control in 2024

Overview: In today's fast-paced life sciences industry, many companies struggle with cumberso..

Date : 20th August 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

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

HR Documentation: How Can HR Professionals and Supervisors Create Litigation Proof Decisions in 2024

HR Documentation: How Can HR Professionals and Supervisors Create Litigation Proof Decisions in 2024

Overview: In the fast-paced world of human resources, documentation isn't just about keeping ..

Date : 08th August 2024

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

Duration : 90 Mins

21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration

21 CFR Part 820 - Quality System Regulation - Applying Principles of Lean Documents and Lean Configuration

Overview: 21 CFR Part 820 delineates the Quality System Regulation (QSR) that governs all ent..

Date : 23rd July 2024

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

Duration : 75 Mins

HR Compliance 101 - For New HR/Non-HR Managers

HR Compliance 101 - For New HR/Non-HR Managers

Overview: In today's complex workplace, HR compliance isn't just a challenge – it's a moving ..

Date : 23rd July 2024

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

Duration : 75 Mins

Best Practices in Preparation for an FDA Computer System Audit in 2024

Best Practices in Preparation for an FDA Computer System Audit in 2024

10 Minutes excerpt from the recorded event for your review: Best Practices in Preparation for a..

Date : 22nd July 2024

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

Duration : 90 Mins

The 6 Most Common Problems in FDA Software Validation and Verification in 2024

The 6 Most Common Problems in FDA Software Validation and Verification in 2024

Overview: Professionals working with FDA-regulated software face numerous challenges when it c..

Date : 18th July 2024

Time : This Event is Over

Duration : 75 Mins

Mastering Mobile App & Medical Device Software Validation and Cybersecurity in FDA-Regulated Environments

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

Virtual and In-Person Onboarding Your New Hire: Policies, Practices, and Processes

Virtual and In-Person Onboarding Your New Hire: Policies, Practices, and Processes

Overview: As we emerge from the pandemic era and adapt to a new normal, the landscape of work..

Date : 27th June 2024

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

Duration : 45 Mins

Human Factors/ Usability Studies following ISO 62366 , the FDA Guidance and the new FDA Draft Guidance

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

Mastering Error Resolution: Reg E vs Nacha Operating Rules

Mastering Error Resolution: Reg E vs Nacha Operating Rules

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

Date : 12th June 2024

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

Duration : 90 Mins

Multi-State Payroll Tax Compliance - June 2024

Multi-State Payroll Tax Compliance - June 2024

Overview: Navigating the complexities of multi-state payroll tax compliance can be a daunting ..

Date : 10th June 2024

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

Duration : 60 Mins

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