Quality Management

Quality management ensures that an organization, product, or service is consistent. It has four main components: Quality Planning, Quality Assurance, Quality Control and Quality Improvement. Quality management is focused not only product and service quality, but also on the means to achieve it. Quality management, therefore, uses quality assurance and control of processed as well as products to achieve more consistent quality. The International Organization for Standardization (ISO) created the Quality Management System (QMS) standards. ISO has several standards that support quality management. The Software Engineering Institute has its own process assessment and improvement methods, called Capability Maturity Model Integration and IDEAL respectively.


$149.00

 August 17 2021

 01 : 00 PM EST    

 120 Minutes

EEOC Report: Workplace Discrimination And Harassment Prevention Not Working-Workplaces Fail To Implement Systemic Changes

You have been in Human Resources or management for years. Your plate is full—too much to do and to know in your increasingly stressful job. You are expected to stay current in discrimination and harassment case law for all the federal and state-protected classes. Are you current? It seems like an unending responsibility. You remember hearing something in the news about a change in the pregnancy law, but can..

$200.00

 Recorded Webinar

 60 Minutes

 Refer a Friend

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.Upon course completion, you will be able to:Define “machine learning”Describe how machine learning is already being used by law firmsEvaluate how Artificial Intelligence is changing legal jobsConsider the ethical implications of Artific..

$200.00

 Recorded Webinar

 90 Minutes

 Refer a Friend

Audit Trail Generation and Review

Computerized systems are used throughout the life sciences industry to support various regulated activities, which in turn generate many types of electronic records. These electronic records must be maintained according to regulatory requirements contained within FDA’s 21 CFR Part 11 for US jurisdictions and Eudralex Volume 4 Annex 11 for EU jurisdictions.One of the requirements for such compliance is the g..

$200.00

 Recorded Webinar

 60 Minutes

 Refer a Friend

Best Practices for Using Your Quality Management System’s Quality Objectives and KPIs for Meaningful Process Improvement

Numbers, data, facts, perfect information all allow us to make more informed less risky decisions in every aspect of our lives. Due to the increased demands and business pressures to do more with fewer resources, decision-makers in every organization are tasked with making fast and informed decisions.Knowing how what to measure, how to measure it, what the data says where you are now, where you want to be i..

$200.00

 Recorded Webinar

 90 Minutes

 Refer a Friend

CAPA, Failure Investigation and Root Cause Analysis to Meet FDA Expectations

Analysis of investigation reports reveals that human error is one of the top root causes for deviations, discrepancies and quality incidents in pharmaceutical manufacturing. And when you examine the CAPA's that are developed from these, retraining and rewrite of SOP is top the list. Yet on further re-examination, you find that these problems keep resurfacing again and again. Put in another way, the CAPA's a..

$200.00

 Recorded Webinar

 60 Minutes

 Refer a Friend

Construction Law from Start to Finish

Whether you are new to the construction practice or are looking for a comprehensive refresher, this course will cover multiple issues that must be taken into consideration in the realm of construction law. Join our experienced faculty as they cover a broad, basic overview of the construction process; the fundamentals of construction contracts and key provisions; the basics of insurance; and the impact chang..

$200.00

 Recorded Webinar

 60 Minutes

 Refer a Friend

Designing an Effective and Efficient Internal Audit Process for Your Quality Management System

This webinar will focus on designing a thorough internal audit set of process tools, accurately captured in your internal audit procedure that will provide many years of payback and dividends for your organization. Areas CoveredUtilizing PDCA before your internal audits9.2.1 internal audit (general requirements)9.2.2 internal audit scope9.2.2 internal audit frequency9.2.2 internal audit methodsInternal Audi..

$200.00

 Recorded Webinar

 60 Minutes

 Refer a Friend

Drafting Document Retention Policies

The presentation reviews the basic approach of Information Governance and the importance of getting the relevant stakeholders at the table when drafting a document retention policy. We discuss the importance of document destruction and how to develop a policy that balances the interests of the various stakeholders.Areas CoveredInformation GovernanceObjectivesPolicies and ProceduresRecords Retention and Dest..

$200.00

 Recorded Webinar

 90 Minutes

 Refer a Friend

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 implementing strategies and practices like operational excellence and performance reliability. To achieve this goal, innovative approaches to traditional processes need to take place. This webinar..

$200.00

 Recorded Webinar

 60 Minutes

 Refer a Friend

How To Navigate Political Speech In The Workplace

Political speech at work is creating more of a problem now than it did during the 2016 Presidential election!!! With the impeachment, divisive country, and upcoming 2020 election, it has escalated even more. A new survey has found that a significantly increased percentage of employees are feeling stressed and strained because of the political speech since the 2016 campaign! Employees are feeling..

$200.00

 Recorded Webinar

 90 Minutes

 Refer a Friend

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 errors start at the design stage. Procedures play a vital role in human reliability. Nevertheless, it is essential to understand human behavior and the psychology of error as well as underst..

$200.00

 Recorded Webinar

 60 Minutes

 Refer a Friend

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

 Recorded Webinar

 90 Minutes

 Refer a Friend

Impaired Loans: Handle with Care - How to Manage, Account For and Collect Them

Impairment in any form of lending is but a usual mishap that will typically occur, as a rule of the game. For bankers, loan impairment is something to prepare for, as early as before setting up operations, and to permanently upgrade. Failure to do that reveals costly. Refusal to do that, though, deprives the bank of lending premiums, in that the bank will not lend to credit-risky borrowers. Hence it is miss..

$200.00

 Recorded Webinar

 90 Minutes

 Refer a Friend

Implementing an Enterprise-wide Risk Management Framework in a Financial Institution

Financial institutions most often inherit some implicit view on their risks and then add elements as time goes by, as mishaps occur and as regulators demand. The result is all too often the spectacle of a claim at consistency, whilst risk priorities are more the result of interdepartmental relationships, and some risks can be misunderstood. However, when setting up a complete framework, pitfalls are legion...

$200.00

 Recorded Webinar

 60 Minutes

 Refer a Friend

Issues in Calibrations and Accuracy in Method Validation

Accuracy, the ability of a methodology to give results within acceptable limits when compared to known values, is a fundamental and key requirement. Calibration is the most common approach to obtain accuracy.Accuracy requires a comparison to a validated material. The level of confidence depends on traceability, a chain connecting the samples of interest all the way to the specific metric standards. This..

Showing 1 to 15 of 40 (3 Pages)