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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

Responding to EEOC Discrimination Charges - What’s Your Business Case in 2026?

Responding to EEOC Discrimination Charges - What’s Your Business Case in 2026?

Overview: The EEOC processed more than 88,000 new discrimination charges in Fiscal Year 2025, ..

Date : 27th May 2026

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

Duration : 75 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

Quality Management System Regulation (QMSR) – Replacement of QSR and Alignment with ISO

Quality Management System Regulation (QMSR) – Replacement of QSR and Alignment with ISO

Overview: Effective February 2, 2026, FDA’s Quality Management System Regulation (QMSR) became..

Date : 23rd April 2026

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

Duration : 90 Mins

California Wage and Hour Laws 2026: New Rules, Overtime, Pay, Leave and Compliance

California Wage and Hour Laws 2026: New Rules, Overtime, Pay, Leave and Compliance

Overview: California employers do not usually get into trouble because they ignore the law ent..

Date : 09th April 2026

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 in 2026

HR Documentation: How Can HR Professionals and Supervisors Create Litigation-Proof Decisions in 2026

Overview: Employee documentation continues to be one of the most sensitive and mishandled area..

Date : 31st March 2026

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

Duration : 90 Mins

Mandatory Paid Sick Leave  Breaking Through the Quagmire and Quandary of Compliance in 2026

Mandatory Paid Sick Leave Breaking Through the Quagmire and Quandary of Compliance in 2026

Overview: Many states and the District of Columbia now require employers to provide paid sick ..

Date : 25th March 2026

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

Duration : 90 Mins

Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR in 2026

Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR in 2026

Overview: In 2026, data integrity and privacy risks don’t sit in one department—they show up ..

Date : 19th March 2026

Time : This Event is Over

Duration : 90 Mins

Employers Should Prepare for Immigration Raids in 2026! This Means More I-9 Audits for Employers by ICE

Employers Should Prepare for Immigration Raids in 2026! This Means More I-9 Audits for Employers by ICE

Overview: Worksite immigration enforcement can turn into an operational crisis faster than mos..

Date : 26th February 2026

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

Duration : 90 Mins

I-9 and E-Verify Regulations Under the Trump Administration

I-9 and E-Verify Regulations Under the Trump Administration

Overview: Since January 2025, employer-side immigration enforcement has escalated in ways that..

Date : 26th February 2026

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

Duration : 90 Mins

Risk-Based Excel Spreadsheet Validation and FDA Compliance - Risk-Based CSV/CSA & Part 11

Risk-Based Excel Spreadsheet Validation and FDA Compliance - Risk-Based CSV/CSA & Part 11

Overview:FDA inspections and audits continue to put a bright spotlight on data integrity—especiall..

Date : 27th January 2026

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

Duration : 90 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

EEOC New Stance on Workplace Harassment - What Employers Must Update in their Policies and Investigations

EEOC New Stance on Workplace Harassment - What Employers Must Update in their Policies and Investigations

Overview: On April 29, 2024, the EEOC issued its first comprehensive workplace-harassment gui..

Date : 25th November 2025

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

Duration : 90 Mins

Transition from CSV to CSA; FDA Final CSA Guidance, September 2025 for Medical Device Manufacturing & Quality Testing

Transition from CSV to CSA; FDA Final CSA Guidance, September 2025 for Medical Device Manufacturing & Quality Testing

Overview: For decades, life-science teams have relied on Computer System Validation (CSV)—sha..

Date : 21st November 2025

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

Duration : 90 Mins

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