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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

Multi-State Payroll: Navigate Taxation and Compliance Challenges

Multi-State Payroll: Navigate Taxation and Compliance Challenges

Overview: The modern workplace has undergone a dramatic transformation. Remote work, once a ni..

Date : 27th January 2025

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

Duration : 60 Mins

What is in Store for Employers When Updating Employee Handbooks in 2025?

What is in Store for Employers When Updating Employee Handbooks in 2025?

Overview: Imagine this: Your employee handbook, a tool designed to guide and protect your org..

Date : 17th January 2025

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

Duration : 90 Mins

THE DOL’s New Rule on Independent Contractors

THE DOL’s New Rule on Independent Contractors

Overview: Misclassifying workers as either independent contractors or employees carries signif..

Date : 16th January 2025

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

Duration : 75 Mins

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligence (AI) and Machine Learning (ML)-

Validation of FDA-Regulated Systems that Incorporate Artificial Intelligence (AI) and Machine Learning (ML)-

Overview: As the life sciences industry, encompassing pharmaceuticals, medical devices, biotech..

Date : 13th January 2025

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

Duration : 90 Mins + Q&A

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

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

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