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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
Preparing a FDA 510(k) submission - What to Know in 2025
Overview: The FDA 510(k) submission process remains one of the most crucial regulatory pathwa..
Date : 26th June 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 75 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
The 6 Most Common Problems in FDA Software Validation and Verification in 2025
Overview: Professionals working with FDA-regulated software face numerous challenges when it co..
Date : 12th June 2025
Time : This Event is Over
Duration : 75 Mins
Multi-State Payroll Tax Compliance in 2025
Overview: Navigating the complexities of multi-state payroll tax compliance can be a daunting ..
Date : 04th June 2025
Time : This Event is Over and the Recorded Content is Available
Duration : 60 Mins
Data Integrity and Privacy Compliance: 21 CFR Part 11, SaaS/Cloud, and EU GDPR for Life Sciences
Overview: In today's rapidly evolving life sciences landscape, ensuring data integrity and pr..
Date : 15th July 2025
Time : 1:00 PM Eastern Time / 10:00 AM Pacific Time
Duration : 75 Mins