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Best Practices for FDA Computer System Audit Preparation in 2026

Best Practices for FDA Computer System Audit Preparation in 2026

Overview: For those of us who have worked around FDA-regulated computer systems for many year..

Date : 29th May 2026

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

Duration : 90 Mins

Medical Device Cybersecurity Following FDA’s 2026 Premarket Guidance

Medical Device Cybersecurity Following FDA’s 2026 Premarket Guidance

Overview Cybersecurity is now a central part of FDA’s review expectations for many connected, ..

Date : 28th May 2026

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

Duration : 60 Mins

The 6 Most Common Problems in FDA Software Validation and Verification in 2026

The 6 Most Common Problems in FDA Software Validation and Verification in 2026

Overview: Software validation and verification remain common sources of compliance risk for F..

Date : 14th May 2026

Time : This Event is Over

Duration : 75 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 : This Event is Over and the Recorded Content is Available

Duration : 75 Mins

Data Integrity and Data Governance for Computer Systems Regulated by FDA in 2025

Data Integrity and Data Governance for Computer Systems Regulated by FDA in 2025

Overview: As regulatory scrutiny intensifies, data integrity and governance have become corne..

Date : 30th May 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

Responding to EEOC Discrimination Charges - What’s Your Business Case in 2025?

Responding to EEOC Discrimination Charges - What’s Your Business Case in 2025?

Overview: Discrimination charges are no longer a fringe risk—they’re a defining workplace chal..

Date : 22nd May 2025

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

Duration : 75 Mins

The 2024 EEO-1 Reporting  Opens on May 20, 2025! Learn What The Changes Are to Be Compliant!

The 2024 EEO-1 Reporting Opens on May 20, 2025! Learn What The Changes Are to Be Compliant!

Overview: The Equal Employment Opportunity Commission (EEOC) has announced that the 2024 EEO-..

Date : 21st May 2025

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

Duration : 90 Mins

Best Practices for Auditing a Vendor of Computer Systems Regulated by FDA

Best Practices for Auditing a Vendor of Computer Systems Regulated by FDA

10 Minutes excerpt from the recorded event for your review:Read the LinkedIn Article: LinkedIn ..

Date : 30th May 2024

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

Duration : 90 Mins

Navigating Employee Terminations: Minimizing Risks and Safeguarding Your Company's Reputation

Navigating Employee Terminations: Minimizing Risks and Safeguarding Your Company's Reputation

8 Minutes excerpt from the recorded event for your review:Read the LinkedIn Article:Navigating Emplo..

Date : 29th May 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

Adapting to DOL's New Salary Thresholds by July 2024

Adapting to DOL's New Salary Thresholds by July 2024

14 Minutes excerpt from the recorded event for your review:Date of Release and Key Changes:On Apri..

Date : 23rd May 2024

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

Duration : 90 Mins

Excel Spreadsheet in FDA Environment - Ensuring Data Integrity and 21 CFR Part 11 Compliance in 2024

Excel Spreadsheet in FDA Environment - Ensuring Data Integrity and 21 CFR Part 11 Compliance in 2024

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

Date : 15th May 2024

Time : This Event is Over

Duration : 90 Mins

Mastering Mobile App Validation in FDA-Regulated Environments

Mastering Mobile App Validation in FDA-Regulated Environments

Overview: In this webinar, we will delve into the critical aspects of applying computer syste..

Date : 26th May 2023

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

Duration : 90 Mins

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