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Detecting Truth, Deception and Lies when Conducting an Workplace Investigation

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

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

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

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

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

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

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

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

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

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

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

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