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.
Validation of FDA-Regulated Systems with AI, ML & LLMs (ChatGPT)
Overview: Life science industries — including pharmaceutical, medical device, biotechnology, ..
Date : 11th September 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
The One Big Beautiful Bill (OBBB) is Now the Law. How Will It Impact the Workplace?
Overview: The "One Big Beautiful Bill," officially titled the One Big Beautiful Bill Act (OBB..
Date : 27th August 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Payroll Record Retention Requirements and How to Become More Electronic
Overview: As technology continues to reshape the workplace, payroll departments are under pre..
Date : 22nd August 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR - 2025
Overview: In today's rapidly evolving life sciences landscape, ensuring data integrity and pr..
Date : 21st August 2025
Time : This Event is Over
Duration : 75 Mins
Best Practices in Preparation for an FDA Computer System Audit in 2025
Overview: In 2025, the FDA's expectations for validated computer systems have never been high..
Date : 31st July 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 Now to Stay Compliant
Overview: With the Trump administration now in office, immigration enforcement has swiftly es..
Date : 22nd July 2025
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 2025
Overview: The U.S. Food and Drug Administration (FDA) plays a critical role in safeguarding pub..
Date : 27th June 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
Preparing a FDA 510(k) submission - What to Know in 2025
Overview: The FDA 510(k) submission process remains one of the most crucial regulatory pathwa..
Date : 26th June 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
HR & Payroll Recordkeeping Compliance | IRS, FLSA & State Laws Explained
Overview: Managing payroll and HR records has evolved from simply maintaining folders in a fil..
Date : 24th June 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
The 6 Most Common Problems in FDA Software Validation and Verification in 2025
Overview: Professionals working with FDA-regulated software face numerous challenges when it co..
Date : 12th June 2025
Time : This Event is Over
Duration : 75 Mins
Multi-State Payroll Tax Compliance in 2025
Overview: Navigating the complexities of multi-state payroll tax compliance can be a daunting ..
Date : 04th June 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Data Integrity and Data Governance for Computer Systems Regulated by FDA in 2025
Overview: As regulatory scrutiny intensifies, data integrity and governance have become corne..
Date : 30th May 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 75 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
Sampling Plans for Verification and Validation, Production Process Validation and Production Control
Overview: When design flaws go unnoticed until late in production—or when a batch fails inspe..
Date : 23rd May 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Responding to EEOC Discrimination Charges - What’s Your Business Case in 2025?
Overview: Discrimination charges are no longer a fringe risk—they’re a defining workplace chal..
Date : 22nd May 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins