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.
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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