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61-75 of 182 results
JUSTIN MUSCOLINO
$
Nov 13, 2025
01:00 PM
EFT Act and Regulations E in 2023
We will explore all aspects of regulation E, plus discuss how this rule impacts your day-to-day responsibilities. You will learn how to comply with the Electronic Fund Transfers Act In 2023.
This webinar will focus on t...
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RONALD A SEREIKA
$
Oct 28, 2025
01:00 PM
Best Practices for Preventing Credit Card Fraud
This Webinar describe
History of credit cards in corporate America - Why companies have decided to use credit cards for their employee’s - How to control cash and spending on credit cards - Pro&rs...
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Mr. Colin Wolf
$
Dec 10, 2025
01:00 PM
HR Analytics: Using Data to Drive Strategic Decision-Making
HR analytics has emerged as a critical function, transforming HR from a traditionally administrative role to a strategic partner. By leveraging data, organizations can gain valuable insights into their workforce, make in...
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GINETTE COLLAZO
$
Jan 01, 2026
01:00 PM
From Training to Human Relia
Pharmaceutical manufacturing sites continuously compete, even within the same company to maintain production volumes and avoid closures. To attain a status of a high performing organization manufacturing sites are implem...
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Mr. Colin Wolf
$
Dec 01, 2025
11:00 AM
Navigating Workplace Power Dynamics: Mastering Influence Without Authority
Workplace power dynamics are a pervasive and often unspoken reality. While formal authority stems from hierarchical positions, influence is a more nuanced and essential skill, particularly for those who seek to lead with...
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GINETTE COLLAZO
$
Jan 01, 2026
01:00 PM
From Training to Human Reliability In Manufacturing
Pharmaceutical manufacturing sites continuously compete, even within the same company to maintain production volumes and avoid closures. To attain a status of a high performing organization manufacturing sites are implem...
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GINETTE COLLAZO
$
Jan 01, 2026
01:00 PM
How to Implement an Effective Human Error Investigation Program
Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikely that human error will ever be eliminated, many human performance problems can be prevented. Human...
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GINETTE COLLAZO
$
Jan 01, 2026
01:00 PM
How to Write SOP’s for Human Error Reduction
Human error is known to be the primary cause of quality and production losses in many industries. Although it is unlikely that human error will ever be eliminated, many human performance problems can be prevented. Human...
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MARK SMITH
$
Dec 26, 2025
03:00 PM
Skill-First Hiring: Why Education and Years of Experience Are Less Important for Many Jobs
Skills-based hiring has been a topic of interest for many businesses and governments for the past few years. But even as interest grows, many hiring managers push back on the idea, worried about the potentially detriment...
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CAROL PTAK
$
Nov 19, 2025
01:00 PM
Adaptive S and OP
Adaptive S&OP is the strategic component of the Demand Driven Adaptive Enterprise (DDAE) Model. Adaptive S&OP is the integrated business process that provides management the ability to strategically define, direc...
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Kelly Thomas
$
Jan 01, 2026
01:00 PM
New FDA Draft Guidance Part 11 Compliance
This webinar describe, As part of the Case for Quality program US FDA noted how an excessive focus by the industry on compliance rather than quality may be diverting resources and management attention toward meeting regu...
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Mark Henriques
$
Oct 31, 2025
03:00 PM
Artificial Intelligence and the Law
In this practical webinar, you will learn about the latest developments in Artificial Intelligence and get a glimpse into the future, as additional legal tasks get automated.
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JOSE IGNACIO MORA
$
Jan 06, 2026
01:00 PM
How to Conduct a Human Factors / Usability Validation?
This webinar will explain the procedure described in ISO62366 and the 2016 FDA Guidance for compliant human factors/usability validation. HF/U validation is very different from device validation. For example, success cri...
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MEREDITH CRABTREE
$
Jan 01, 2026
01:00 PM
5 Key Components of Good Manufacturing Practices to obtain cGMP certification
Pharmaceutical and other FDA-regulated industries are tasked with safely manufacturing products for people (or animals) around the world. The FDA has set specific requirements, known as cGMPs) for facilities to meet the...
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Angela Bazigos
$
Nov 13, 2025
03:00 PM
Audit Trail Generation and Review
This webinar will demystify audit trails and describe the benefits of an audit trail for your company. Attendees will the tools required to generate compliant audit trails on a domestic and international basis and will a...
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