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Payroll Record Retention Requirements and How to Become More Electronic

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

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

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

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

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

HR & Payroll Recordkeeping Compliance | IRS, FLSA & State Laws Explained

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

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

Sampling Plans for Verification and Validation, Production Process Validation and Production Control

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

Excel Spreadsheet in FDA Regulated Environment - Ensuring Data Integrity and 21 CFR Part 11 Compliance in 2025

Excel Spreadsheet in FDA Regulated Environment - Ensuring Data Integrity and 21 CFR Part 11 Compliance in 2025

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

Date : 11th April 2025

Time : This Event is Over

Duration : 90 Mins

Complying with I-9 and E-Verify Regulations Under the New Administration

Complying with I-9 and E-Verify Regulations Under the New Administration

Overview Since the start of 2025, immigration enforcement has intensified at an unprecedented ..

Date : 26th March 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

Best Practices for Creating a Clear-Cut Contract and Service Level Agreement (SLA) with a Vendor of Computer Systems Regulated by FDA

Best Practices for Creating a Clear-Cut Contract and Service Level Agreement (SLA) with a Vendor of Computer Systems Regulated by FDA

Overview: Selecting and managing a vendor for computer systems in FDA-regulated environments ..

Date : February 26, 2025

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

Duration : 90 Mins

Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR in 2025

Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR in 2025

Overview: In today's rapidly evolving life sciences landscape, ensuring data integrity and priv..

Date : 14th February 2025

Time : This Event is Over

Duration : 90 Mins

US FDA Requirements for Medical Products Labeling / UDI

US FDA Requirements for Medical Products Labeling / UDI

Overview: The world of medical product labeling in the United States is governed by a complex ..

Date : 10th February 2025

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

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