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Independent Contractor vs. Employee And the New Rules Issued by The Department of Labor

Independent Contractor vs. Employee And the New Rules Issued by The Department of Labor

Overview: For HR professionals, payroll leaders, managers, and business owners, worker classi..

Date : 29th April 2026

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

Duration : 75 Mins

FDA’s QMSR is Coming: Practical Readiness for Quality Teams

FDA’s QMSR is Coming: Practical Readiness for Quality Teams

Overview: With the FDA’s Quality Management System Regulation (QMSR) taking effect in February..

Date : 21st January 2026

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

Duration : 60 Mins

Employee Expense Reimbursements: IRS Rules, Accountable Plans, Per Diems & OBBB Updates

Employee Expense Reimbursements: IRS Rules, Accountable Plans, Per Diems & OBBB Updates

Overview: Employee expense reimbursements may seem straightforward, but when handled incorrect..

Date : 15th September 2025

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

Duration : 75 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 Guidance for Use of Social Media by Regulated Industries

FDA Guidance for Use of Social Media by Regulated Industries

Overview: In the early days of social media, regulatory agencies were observers — watching as..

Date : 30th April 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 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

Effective Technical Writing for Medical Devices: Improving Your Skills for Clear and Concise Communication

Effective Technical Writing for Medical Devices: Improving Your Skills for Clear and Concise Communication

Overview: In the world of medical device manufacturing, technical writing is more than just a..

Date : 27th March 2025

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

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

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

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

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

Medical Device Software Verification and Validation Following FDA 2023 Guidance and ISO 62304

Medical Device Software Verification and Validation Following FDA 2023 Guidance and ISO 62304

Overview: In the fast-evolving field of medical technology, ensuring the safety and efficacy ..

Date : 28th May 2024

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

Duration : 60 Mins

Excel Spreadsheet in FDA Regulated Environment in 2023

Excel Spreadsheet in FDA Regulated Environment in 2023

Overview:The use of Excel in FDA-regulated environments goes beyond typical data organization and ..

Date : 27th July 2023

Time : This Event is Over

Duration : 90 Mins

Form 941 in 2026: Avoid Payroll Tax Errors, Corrections and IRS Notices

Form 941 in 2026: Avoid Payroll Tax Errors, Corrections and IRS Notices

Overview Form 941 is familiar to every employer, but that familiarity often creates a false s..

Date : 07th May 2026

Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time

Duration : 75 Mins

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