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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
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
Prepare for FDA QMSR Inspections: 483 & Warning Letter Response
Overview: FDA inspections under the new QMSR can look and feel different—not just in what inv..
Date : 23rd February 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
ISO 13485:2016 Utilizing Principles of Lean Documents and Lean Configuration
Overview: Medical device and life science organizations are expected to maintain a Quality Ma..
Date : 20th February 2026
Time : This Event is Over and the Recorded Content is Available
Duration : 75 Mins
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
Excel Spreadsheet in FDA Regulated Environment - Validating Excel for GxP & 21 CFR Part 11
Overview: The use of Excel in FDA-regulated environments goes far beyond basic analysis. When ..
Date : 21st November 2025
Time : This Event is Over
Duration : 75 Mins
Clinical Trial Systems: Trial Master File (TMF) and eTMF, & FDA’s Recent Draft Guidance for Electronic Records/Signatures Used in Clinical Trials
Overview: Organizations involved in the conduct of human clinical trials must meet rigorous re..
Date : 30th September 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
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
Payroll Record Retention Requirements and How to Become More Electronic
Overview: As technology continues to reshape the workplace, payroll departments are under pre..
Date : 22nd August 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Data Integrity and Privacy - Compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR - 2025
Overview: In today's rapidly evolving life sciences landscape, ensuring data integrity and pr..
Date : 21st August 2025
Time : This Event is Over
Duration : 75 Mins
Best Practices in Preparation for an FDA Computer System Audit in 2025
Overview: In 2025, the FDA's expectations for validated computer systems have never been high..
Date : 31st July 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 90 Mins
I-9 Audits & ICE Workplace Raids: What Employers Must Do Now to Stay Compliant
Overview: With the Trump administration now in office, immigration enforcement has swiftly es..
Date : 22nd July 2025
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 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
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 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