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Home › Online Training ›  QA/QC

Quality Assurance and Quality Controls Training - Live Webinars, Recordings & CDs

Whether you are a quality assurance or a quality control professional, you know how the rapid transformations in regulatory requirements and technology are changing the nature of your work. We understand this challenge and have put together quality assurance and quality control courses to help you make your role robust-proof. Browse for the many courses, standards, and tools of specific interest to you.
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Recorded/CD
Basic Statistics for Microbiological Sampling

Basic Statistics for Microbiological Sampling

  • Speaker: Jim Dickson
  • Product ID: 702682
  • Duration: 90 Min
This webinar will address the statistical basis for sampling and testing. Topics will include two and three class sampling plans, as well as the operating characteristics of individual plans with primary focus on interpretation of results, based on the limitations of sampling plans and microbiological methods.
CD/Recorded
$50
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Recorded/CD
Smoking and Curing of Meat as a Food Preservative - Techniques and Methods

Smoking and Curing of Meat as a Food Preservative - Techniques and Methods

  • Speaker: Jeffery Giesberg
  • Product ID: 702764
  • Duration: 60 Min
This training on preserving meat will explore the techniques and methods of smoking and curing meats commercially and its benefits, health risks and HACCP requirements. It will also cover packaging, storage and shipping considerations for mass produced cured meats.
CD/Recorded
$299
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Recorded/CD
Foreign Material Control in Food Processing

Foreign Material Control in Food Processing

  • Speaker: Melinda Allen
  • Product ID: 702699
  • Duration: 60 Min
This webinar for food processing will cover the overview of systems necessary to reduce the risk of foreign material contamination, associated guidelines, HACCP and prerequisite programs followed by investigative techniques and a customer and team response plan.
CD/Recorded
$229
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Recorded/CD
Process Validation for Medical Devices - The Regulatory Approach

Process Validation for Medical Devices - The Regulatory Approach

  • Speaker: Dan OLeary
  • Product ID: 702673
  • Duration: 90 Min
This medical device process validation training will use recent warning letters to explain the regulatory requirements for process validation and what FDA Investigators look for. It will cover process validation components (IQ, OQ, and PQ), and the content of protocols and reports.
CD/Recorded
$229
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Recorded/CD
Microbiological Sampling of Foods

Microbiological Sampling of Foods

  • Speaker: Jim Dickson
  • Product ID: 702659
  • Duration: 60 Min
This webinar on microbiological sampling for foods will address fundamental approaches to sampling, from raw materials to finished products. Topics will include sampling plans, sample collection methods and chain of custody issues. A primary focus will be on interpretation of results, based on the limitations of sampling plans and microbiological methods.
CD/Recorded
$229
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Recorded/CD
Product Complaint Investigations - The application of Lean Six Sigma methodology for U.S. FDA-Regulated Industries

Product Complaint Investigations - The application of Lean Six Sigma methodology for U.S. FDA-Regulated Industries

  • Speaker: Shahbaz Shahbazi,Ray Bandziulis
  • Product ID: 702614
  • Duration: 75 Min
This webinar will discuss the use of Lean Six Sigma methodology for product complaint investigations and offer a standardized approach for FDA regulated life science companies to follow whenever product complaint investigations are needed.
CD/Recorded
$229
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Recorded/CD
Fast and Proven Accounts Receivable Collection Techniques

Fast and Proven Accounts Receivable Collection Techniques

  • Speaker: Steven Gan
  • Product ID: 702584
  • Duration: 120 Min
The Accounts Receivable Collection Webinar covers information on collection activities, types of debtors, payment/non-payment issues and how to establish a positive dialogue. Presenter will teach in the form of several role play situations that contain collection challenges requiring the participants to analyze and formulate collection strategies and resolutions.
CD/Recorded
$249
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Recorded/CD
HACCP Webinar: Setting up HACCP Plans for Small Companies

HACCP Webinar: Setting up HACCP Plans for Small Companies

  • Speaker: David Armatis
  • Product ID: 702566
  • Duration: 60 Min
This 60 minute webinar will cover the details on middle and final efforts for setting up a food safety and HACCP program for your organization. You will learn and develop skill sets to manage and influence an integrated program intended to reduce potential food safety risk.
CD/Recorded
$229
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Recorded/CD
Adjusting your Compliance Program to Meet new FDA Requirements

Adjusting your Compliance Program to Meet new FDA Requirements

  • Speaker: Jason Mefford
  • Product ID: 702509
  • Duration: 60 Min
This webinar will help you understand the new FDA requirements related to the FDA Food Safety Modernization Act (FSMA). You will learn how companies must change their compliance programs in order to meet these new requirements.
CD/Recorded
$229
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Recorded/CD
Effective Use of Validation and Verification to Improve your Food Safety Management System

Effective Use of Validation and Verification to Improve your Food Safety Management System

  • Speaker: John Surak
  • Product ID: 702458
  • Duration: 60 Min
This webinar will cover strategies to effectively use the proper validation and verification techniques to increase the effectiveness of a FSMS. It will show how any food or pharmaceutical company can properly use these techniques to ensure compliance with either ISO 22000 or ISO 9001.
CD/Recorded
$149
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Recorded/CD
To Validate or Not To Validate: A Daily Question for the Pharmaceutical Scientist

To Validate or Not To Validate: A Daily Question for the Pharmaceutical Scientist

  • Speaker: Kim Huynh-Ba
  • Product ID: 702386
  • Duration: 90 Min
This 90-minute webinar will outline the common deficiencies in relation to method validation, for pharmaceutical products, outline regulatory requirements and the change control process needed to stay in compliance.
CD/Recorded
$0
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Recorded/CD
(QMS) Competence and Training Requirements per FDA QSR and ISO 13485

(QMS) Competence and Training Requirements per FDA QSR and ISO 13485

  • Speaker: Daniel O Leary
  • Product ID: 702376
  • Duration: 90 Min
This 90-minute webinar will help you understand the competence and training requirements in the Quality Management Systems for medical devices, especially FDA QSR, ISO 13485, and even ISO 9001.
CD/Recorded
$229
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Recorded/CD
QbD Approach to Analytical Method Lifecycle: Design, Development, Validation, Transfer

QbD Approach to Analytical Method Lifecycle: Design, Development, Validation, Transfer

  • Speaker: Gregory Martin
  • Product ID: 702278
  • Duration: 120 Min
This 120-minute webinar on using the QbD Approach to Analytical Method Lifecycle is designed to provide participants with a lifecycle approach to developing and validating analytical methods and comply with compendial requirements.
CD/Recorded
$149
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Recorded/CD
Avoiding the 90 Percentage Syndrome: Why Software Project Status Reports are Often Wrong (and What You Can Do About It)

Avoiding the 90 Percentage Syndrome: Why Software Project Status Reports are Often Wrong (and What You Can Do About It)

  • Speaker: Gary Gack
  • Product ID: 702107
  • Duration: 90 Min
This Software Project Management training is designed to help executives and managers set and deliver on appropriate and realistic expectations, and avoid the 90% Syndrome.
CD/Recorded
$499
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Recorded/CD
Science-based (Software) Test Planning - Fewer Tests, Better Coverage

Science-based (Software) Test Planning - Fewer Tests, Better Coverage

  • Speaker: Gary Gack
  • Product ID: 702109
  • Duration: 90 Min
This Software Testing training will review a testing method based on 'Design of Experiments' to greatly reduce redundant test cases and ensure that maximum number of defects are found.
CD/Recorded
$499
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Recorded/CD
Good manufacturing practices for food contact packaging producers in the US and EU

Good manufacturing practices for food contact packaging producers in the US and EU

  • Speaker: Thomas J. Dunn
  • Product ID: 701959
  • Duration: 57 Min
This food safety webinar addresses components of Good Manufacturing Practices that packaging material suppliers should follow for adherence to both regulatory and voluntary standards protocols
CD/Recorded
$549
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Recorded/CD
Critical Role of Quality Audit in GxP Compliance & Improvement

Critical Role of Quality Audit in GxP Compliance & Improvement

  • Speaker: David Dills
  • Product ID: 700982
  • Duration: 62 Min
This Webinar will address the key elements on being an effective auditor for your company covering the different types of audits, what do audits measure and how are audit results measured and certainly why perform audits to begin with. Learn the basic skills required and how to apply them and the knowledge in becoming more effective.
CD/Recorded
$299
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Recorded/CD
Acceptance Sampling Plans for Process Validation and Production Lot Monitoring

Acceptance Sampling Plans for Process Validation and Production Lot Monitoring

  • Speaker: Steven Wachs
  • Product ID: 704315
  • Duration: 90 Min
This webinar provides details regarding the generation of acceptance sampling plans often used in process validation and production control to ensure quality of final products. By attending this webinar, participants will be able understand the key inputs and issues involved in determining acceptance sampling plans. Sampling plans for attribute data are the primary focus although variable acceptance sampling plans are presented as well.
CD/Recorded
$0
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Recorded/CD
Record Keeping for a food Recall: Keeping Records to Minimize the Affect of a Recall

Record Keeping for a food Recall: Keeping Records to Minimize the Affect of a Recall

  • Speaker: Craig Nelson
  • Product ID: 701119
  • Duration: 60 Min
This Food safety training will provide valuable guidance to management, supervision, and quality staff that are involved with record keeping for product and ingredient traceability and recall.
CD/Recorded
$199
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Recorded/CD
Aerospace - transitioning to AS9100 Rev.C - Effect of Addition of Risk Management requirements

Aerospace - transitioning to AS9100 Rev.C - Effect of Addition of Risk Management requirements

  • Speaker: Rick Saldivar
  • Product ID: 701299
  • Duration: 75 Min
This AS9100 Rev.C training will cover the changes made in Rev.C and how it might impact your organization including the additional requirements associated with Risk Management.
CD/Recorded
$199
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