$200.00
Drafting Document Retention Policies

 Recorded Webinar
 90 Minutes
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Drafting Document Retention Policies

Companies are overflowing with information. Data is generated at a remarkable rate. What can be kept? What can be destroyed? This timely information helps the persons responsible for drafting document retention policies define the key objectives of the policy and satisfy the necessary legal requirements. Learn the proper elements of legal hold and the consequences for failing to properly implement such hold..

$200.00
Human Factors Validation Testing Following ISO 62366 and new FDA Guidance

 Recorded Webinar
 60 Minutes
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Human Factors Validation Testing Following ISO 62366 and new FDA Guidance

Following the implementation of the results of a Human Factors/ Usability study, a validation of the safety and effectiveness of the use of the device must be conducted. We will explain the FDA required the number of validation participants from each "distinct user population". We will explain how to choose the tests to be conducted and the studies that must be completed prior to the actual validation test...

$200.00
Introduction to Statistical Process Control

 Recorded Webinar
 60 Minutes
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Introduction to Statistical Process Control

This webinar will introduce attendees to the foundations of statistical process control (SPC), including the effects of variation and accuracy on process quality. The definition of a Six Sigma process will be illustrated. Attendees will learn how to construct SPC charts that provide visual controls (easily understood signals) that tell production workers when the process requires adjustment to prevent the m..

$200.00
A Leer, A Pat, A Joke, A Gesture, An Innuendo, A Kiss: Are You Prepared To Be the Next Social Media Blitz, Identified on #MeToo, or a Headline in the Newspaper?

 Recorded Webinar
 90 Minutes
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A Leer, A Pat, A Joke, A Gesture, An Innuendo, A Kiss: Are You Prepared To Be the Next Social Media Blitz, Identified on #MeToo, or a Headline in the Newspaper?

Harvey Weinstein, Matt Lauer, Charlie Rose, Al Franken, Garrison Keillor, members of Congress, and various State lawmakers have been accused of sexual harassment and/or sexual assault. But there is a difference between pulling one’s pants down in front of a female colleague at work and touching a woman on her buttocks during a photo op—isn’t there? What is that difference? Are both examples considered sexua..

$200.00
Quality by Design (QbD) for Analytical Methods

 Recorded Webinar
 60 Minutes
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Quality by Design (QbD) for Analytical Methods

This 60-minute presentation will highlight the use of statistical tools to monitor operations for a proactive operation.There are always certain steps in a method where control is critical either because this step contributes a lot to the overall uncertainty or its uncertainty is more likely to change from common causes. These critical points can be assessed and a monitoring program instituted. This data is..

$200.00
Acceptance Sampling for Variables: ANSI/ASQ Z1.9

 Recorded Webinar
 60 Minutes
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Acceptance Sampling for Variables: ANSI/ASQ Z1.9

This webinar will show how to use ANSI/ASQ Z1.9 (formerly MIL-STD 414) to define sampling plans for products with continuous-scale (variables) data, and use the accompanying switching rules to move between normal, reduced, and tightened inspection as required by the publication.ANSI/ASQ Z1.9 (formerly MIL-STD 414) is a widely accepted standard for sampling by variables (continuous scale measurements). The s..

$149.00
How to Set up an Internal Audit Program

 27 February 2019
 02 : 00 PM EST    
 60 Minutes
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How to Set up an Internal Audit Program

An overview of how to set up an internal audit program to address quality management system standards, government regulations, risk management as well as usage for continuous improvement.This is especially useful for small to medium-sized medical device companies and start-up companies to ensure that all of the applicable regulatory requirements are incorporated into the system to ensure compliance with all..

$149.00
Improve Your IRS Compliance: Use Best Practices for TIN Solicitation

 27 February 2019
 02 : 00 PM EST    
 90 Minutes
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Improve Your IRS Compliance: Use Best Practices for TIN Solicitation

This IRS regulatory compliance training will explain the Best TIN Solicitation Best Practices. While TIN solicitation might sound too lascivious for the legitimate business world, it is critical that every organization take this task seriously. For if they don't, a very uncomfortable and costly audit with the IRS is likely to ensue.Areas CoveredIdentify all required TIN information you need to collectDesign..

$200.00
The Dynamic Control Plan

 Recorded Webinar
 60 Minutes
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The Dynamic Control Plan

Failure mode effects analysis (FMEA) and the control plan are both parts of advanced quality planning (AQP). FMEA, in fact, defines the control points or critical nodes of the control plan; process activities that must be controlled to ensure conformance of the critical to quality (CTQ) product characteristics. The dynamic control plan is a natural combination of the process FMEA and control plan into a sin..

$149.00
Adaptive S&OP

 14 March 2019
 01 : 00 PM EST    
 90 Minutes
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Adaptive S&OP

Companies are facing an ever more increasingly complex environment coupled with increasing marketplace volatility. This is causing companies to strive to be more flexible and responsive by streamlining both planning and execution. In addition, companies are attempting to conserve the use of their valuable resources. Instead of investing in products prematurely that then creates an inventory that may not be ..

$149.00
Getting Good VOC, Efficiently: Design Research in the D3® Process

 02 April 2019
 02 : 00 PM EST    
 60 Minutes
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Getting Good VOC, Efficiently: Design Research in the D3® Process

Engineering is extremely integral to user/market adoption. A product to market is difficult whether you are a struggling startup or an established original equipment manufacturer (OEM). Understanding some of the tools available on the front end of product development might help you avoid downstream problems before they become time and money wasters. Gathering good VOC data is one such tool. Usability relate..

$149.00
DDMRP – What Is It?

 08 April 2019
 01 : 00 PM EST    
 90 Minutes
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DDMRP – What Is It?

Companies are facing an ever more increasingly complex environment coupled with increasing marketplace volatility. This is causing companies to strive to be more flexible and responsive by streamlining both planning and execution. In addition, companies are attempting to conserve the use of their valuable resources. Instead of investing in products prematurely that then creates an inventory that may not be ..

$149.00
New National Bioengineered Food Disclosure Act (GMO Food Labeling)

 07 May 2019
 01 : 00 PM EST    
 60 Minutes
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New National Bioengineered Food Disclosure Act (GMO Food Labeling)

The new rule is highly anticipated by industry and will hopefully bring clarity to the long-standing GMO questions, cover financial and risk impact to businesses as well as helping consumers with educated food choices based on science, in short session encapsulates everything industry needs to know on launching the (NBFDSA).Learning Objectives Background on US GMO (Genetically Modified Organism) LabelingBas..

$149.00
Demand Driven Adaptive Enterprise

 21 May 2019
 01 : 00 PM EST    
 90 Minutes
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Demand Driven Adaptive Enterprise

The Demand-Driven Adaptive Enterprise model is a management and operational model designed to enable enterprises to adapt to complex and volatile environments. The model utilizes a constant system of innovation and feedback between three primary components; a Demand Driven Operating Model, Demand Driven S&OP and Adaptive S&OP. A Demand-Driven Adaptive Enterprise focuses on the protection and promoti..

$300.00
Audit Report Writing

 27 SEPTEMBER 2018
 04 : 00 PM EST    
 120 Minutes
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Audit Report Writing

Audit Reports can significantly lose their effect if not written professionally. Writing an audit report is a fine art and, once perfected, can take on more importance than the audit itself. In this course, attendees will learn, in-depth, about each component of an audit report and how to set the correct tense and clarity to gain the most effectiveness.Audit Report Structure a. Executive Summary b..

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