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Multi-State Payroll Tax Compliance in 2024 - Navigating Complexities

Multi-State Payroll Tax Compliance in 2024 - Navigating Complexities

Overview In the dynamic and interconnected business environment of 2024, multi-state payroll ..

Date : 17th April 2024

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

Duration : 60 Mins

I-9 Compliance 2024: Corrections, Audits, and Best Practices

I-9 Compliance 2024: Corrections, Audits, and Best Practices

Overview In 2024, employers and HR professionals are navigating the complexities introduced b..

Date : 03rd April 2024

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

Duration : 90 Mins

Nacha Rule – Third-Party Sender (TPS) Roles and Responsibilities - What to Know

Nacha Rule – Third-Party Sender (TPS) Roles and Responsibilities - What to Know

Overview: In 2022, Nacha implemented significant updates to its Operating Rules to enhance cl..

Date : 20th March 2024

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

Duration : 90 Mins

March 2024 Deadline: Understanding DOL's New Independent Contractor Classification Rule

March 2024 Deadline: Understanding DOL's New Independent Contractor Classification Rule

Overview: The upcoming 2024 Independent Contractor Rule by the U.S. Department of Labor (DOL) ..

Date : 29th February 2024

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

Duration : 90 Mins

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

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

Overview: In the high-stakes world of human resources, documentation is more than just paperw..

Date : 16th October 2023

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

Duration : 90 Mins

EEO-1 Reporting Deadline Established For 2023! Prepare for Compliance!

EEO-1 Reporting Deadline Established For 2023! Prepare for Compliance!

Overview: The EEO-1 reporting deadline has become a moving target, so covered employers need ..

Date : 20th June 2023

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

Duration : 90 Mins

Good Documentation Practices to Support FDA Computer System Validation

Good Documentation Practices to Support FDA Computer System Validation

Overview: Computer system validation has been regulated by FDA for more than 30 years, as it ..

Date : 29th March 2023

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

Duration : 90 Mins

FDA Technology Modernization Action Plan (TMAP) and Impact on Regulated Computer Systems and Data

FDA Technology Modernization Action Plan (TMAP) and Impact on Regulated Computer Systems and Data

Overview: Computer system validation has been regulated by FDA for more than 30 years, as it re..

Date : 23rd February 2023

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

Duration : 90 Mins

How to Conduct a Human Factors Usability Validation for Medical Device Products

How to Conduct a Human Factors Usability Validation for Medical Device Products

Course Level: IntermediateOverview:Human Factors/ Usability is the analysis of how people interact ..

Date : 08th Feb 2023

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

Duration : 60 Mins

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

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

Overview: FDA has substantial authority to oversee regulated companies and their operations.&n..

Date : 30th November 2022

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

Duration : 90 Mins

Simplifying the Complexities of the  Family and Medical Leave Act

Simplifying the Complexities of the Family and Medical Leave Act

Overview: The Family and Medical Leave Act is probably THE most complex piece of federal empl..

Date : 26th October 2022

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

Duration : 75 Mins

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

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

Overview: Human Factors/ Usability is the analysis of how people interact with medical devices...

Date : 23rd September 2022

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

Duration : 60 Mins

Water Systems in Pharmaceutical Manufacturing Industry

Water Systems in Pharmaceutical Manufacturing Industry

Overview: This seminar will provide an overview of water systems used for pharmaceutical manu..

Date : 22nd September 2022

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

Duration : 60 Mins

Best Practices in Preparation for an FDA Computer System Audit

Best Practices in Preparation for an FDA Computer System Audit

Overview: FDA requires that all computer systems used to produce, manage and report on “GxP” (G..

Date : 23rd June 2022

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

Duration : 90 Mins

FDA Technology Modernization Action Plan and Impact on Regulated Computer Systems

FDA Technology Modernization Action Plan and Impact on Regulated Computer Systems

Overview: Computer system validation has been regulated by FDA for more than 30 years, as it re..

Date : 31st May 2022

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

Duration : 1 Hour 30 Mins

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