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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
Vendor Qualification for Quality Services

Vendor Qualification for Quality Services

  • Speaker: Todd Graham
  • Product ID: 705285
  • Duration: 60 Min
This webinar will teach you how and when to implement complimentary activities to an outsourced quality function and how to integrate this information into a fully-functioning program.
CD/Recorded
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Recorded/CD
FDA vs Health Canada

FDA vs Health Canada

  • Speaker: Rachelle D Souza
  • Product ID: 704862
  • Duration: 60 Min
This webinar will provide an understanding of the organizational hierarchy of FDA and Health Canada, your regulatory and quality compliance obligations and the implications of the interactions between these two agencies on your organization.
CD/Recorded
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Recorded/CD
Regulatory Compliance for Dietary Supplements in the US, EU, and Canada

Regulatory Compliance for Dietary Supplements in the US, EU, and Canada

  • Speaker: Derrick Swint
  • Product ID: 705238
  • Duration: 90 Min
This training program will offer an understanding of how dietary supplements are regulated differently in the US, EU, and Canada, with a focus on challenges and opportunities in each of these regions. The course will provide an overview of the regulatory agencies that govern requirements within each region and the role that each agency plays in setting and enforcing rules for dietary supplements.
CD/Recorded
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Recorded/CD
Creating and Maintaining an Effective and Efficient Technical Training Programs

Creating and Maintaining an Effective and Efficient Technical Training Programs

  • Speaker: Ginette M Collazo
  • Product ID: 704373
  • Duration: 90 Min
This training program will analyze key elements of training programs in regulated environment. It will also list key performance indicators related to training and offer best practices for developing technical training programs to improve their effectiveness.
CD/Recorded
$249
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Recorded/CD
Understanding the Basics of the FDA's New Labeling Requirements

Understanding the Basics of the FDA's New Labeling Requirements

  • Speaker: Derrick Swint
  • Product ID: 705235
  • Duration: 90 Min
The online training will offer food manufacturers a 360 degree approach to food nutritional labeling from a past, present, and future perspective.
CD/Recorded
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Recorded/CD
How to Perform Measurement Systems Analysis

How to Perform Measurement Systems Analysis

  • Speaker: William Levinson
  • Product ID: 705227
  • Duration: 60 Min
This training program will provide an overview of Measurement Systems Analysis (MSA) including best practices for performing MSA. It will help attendees understand difference between calibration and precision, components of gage capability, procedure for a gage reproducibility and repeatability study and much more.
CD/Recorded
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Recorded/CD
Bio-Relevant Drug Dissolution Testing: A New Simple and Practical Approach

Bio-Relevant Drug Dissolution Testing: A New Simple and Practical Approach

  • Speaker: Saeed Qureshi
  • Product ID: 705256
  • Duration: 120 Min
This training program will highlight the current difficulties in conducting the dissolution tests, and then providing a simple and practical solution so that products could be evaluated appropriately and efficiently.
CD/Recorded
$279
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Recorded/CD
Medical Device vs. Consumer Device: Leveraging Technology to Help Patients and Caregivers

Medical Device vs. Consumer Device: Leveraging Technology to Help Patients and Caregivers

  • Speaker: Tom Kramer
  • Product ID: 705223
  • Duration: 60 Min
This training program will provide an understanding of key areas of design focus for medical wearables. Attendees will learn best practices to implement product development plan that apply to medical devices.
CD/Recorded
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Recorded/CD
3-Hour Virtual Training: Lean and the Manufacturing Process

3-Hour Virtual Training: Lean and the Manufacturing Process

  • Speaker: Charles H Paul
  • Product ID: 705229
  • Duration: 180 Min
Lean implementation is not confined to just manufacturing. It can be appropriately applied throughout the organization in all functions. This virtual training program, however, focuses on manufacturing, where lean was born. The difference between this treatment of lean application and others is that we have imbedded the concept of GMP and compliance into our lean model to make it particularly applicable to the life sciences.
CD/Recorded
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Recorded/CD
Good Manufacturing Practices (GMPs) for Phase I Investigational Drugs / Clinical Studies

Good Manufacturing Practices (GMPs) for Phase I Investigational Drugs / Clinical Studies

  • Speaker: Peggy Berry
  • Product ID: 705255
  • Duration: 90 Min
This webinar will help attendees understand differences between GMP requirements for early and later stage clinical development. It will explore and discuss ways to develop and implement strategies for early GMPs for phase I clinical studies.
CD/Recorded
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Recorded/CD
UDI in the EU – A Preliminary Look

UDI in the EU – A Preliminary Look

  • Speaker: Daniel O Leary
  • Product ID: 704854
  • Duration: 90 Min
Many companies offer their devices in the EU, so must comply with the EU UDI regulations. There are significant differences from the US system. While some details remain, there is sufficient information to allow companies to start planning. This webinar can help you prepare for this major aspect of the new EU regulations.
CD/Recorded
$279
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Recorded/CD
The Canadian Food Label

The Canadian Food Label

  • Speaker: Derrick Swint,Abdesselam Benlembarek
  • Product ID: 705209
  • Duration: 90 Min
The food label is one of the most important tools Canadian consumers can use to make informed choices about healthy and safe foods. Canadian food legislation has specific requirements for food manufacturers regarding what to include on a food label and how it should be presented. This course will review the basic requirements of the Canadian Food label, including requirements for the location and size of the common name, net quantity declaration, list of ingredients and allergen labeling, identity and principal place of business, date markings, nutritional labeling, bilingual requirements, irradiation, and sweeteners. For manufacturers of food products for consumption in Canada wishing to ensure compliance to the latest nutritional labeling standard, this course offers an overview of the necessary elements to ensure compliance.
CD/Recorded
$229
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Recorded/CD
Creating FDA-compliant Microbial Contamination Control Program for Biopharmaceutical Manufacturing

Creating FDA-compliant Microbial Contamination Control Program for Biopharmaceutical Manufacturing

  • Speaker: Henry Urbach
  • Product ID: 703474
  • Duration: 90 Min
This webinar will enable participants to understand sources of contamination and to investigate various contamination issues in the biopharmaceutical manufacturing of sterile and non-sterile products. Learn how to create an effective Environmental Monitoring (EM) program.
CD/Recorded
$249
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Recorded/CD
Food Safety and Quality Management - Effective Incident Tracking

Food Safety and Quality Management - Effective Incident Tracking

  • Speaker: Felix Amiri
  • Product ID: 705204
  • Duration: 2.5 hrs
This Food Safety and Quality Management training will provide guidance on methods for conducting effective incident tracking. Attendees will learn how to analyze and utilize incident tracing information and data to the benefit of your food business.
CD/Recorded
$0
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Recorded/CD
Medical Device Cybersecurity Following New FDA Guidance

Medical Device Cybersecurity Following New FDA Guidance

  • Speaker: Edwin Waldbusser
  • Product ID: 705200
  • Duration: 60 Min
This training will discuss the final guidance on postmarket management of cybersecurity in medical devices which was released in Dec. 2016. Attendees will learn how to establish a risk-based framework for assessing when changes to medical devices for cybersecurity vulnerabilities require reporting to the FDA.
CD/Recorded
$179
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Recorded/CD
Overview of Changes in ISO 13485: 2016

Overview of Changes in ISO 13485: 2016

  • Speaker: Lena Cordie Bancroft
  • Product ID: 704756
  • Duration: 60 Min
This training program will discuss changes from ISO 13485: 2003 to ISO 13485: 2016. Attendees will learn how to apply additional supplier controls and understand how improvement and corrective action clauses are strengthened.
CD/Recorded
$249
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Recorded/CD
Clean Labeling and Natural Food Additives: How to meet consumer demand without compromising functionality, safety, shelf-stability, ethics and regulation

Clean Labeling and Natural Food Additives: How to meet consumer demand without compromising functionality, safety, shelf-stability, ethics and regulation

  • Speaker: Azadeh Namvar
  • Product ID: 705194
  • Duration: 60 Min
This online training will discuss the concept of Clean Labelling. Attendees will learn how to identify the approaches to meet consumer demand without compromising functionality, safety, shelf-stability, ethics and regulation.
CD/Recorded
$0
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Recorded/CD
How to Design and Implement a Dynamic Control Plan

How to Design and Implement a Dynamic Control Plan

  • Speaker: William Levinson
  • Product ID: 705171
  • Duration: 90 Min
Learn how the FMEA and control plan can be combined to create a dynamic control plan, a living document that helps to drive continual improvement.
CD/Recorded
$199
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Recorded/CD
How Create a Value-added cGMP/ISO 13485 Internal/Supplier Auditing System

How Create a Value-added cGMP/ISO 13485 Internal/Supplier Auditing System

  • Speaker: Betty Lane
  • Product ID: 705165
  • Duration: 60 Min
This webinar will cover creating of a value-added an internal and supplier auditing program for compliance to FDA and ISO 13485 internal auditing requirements. It will include how to set up and manage the auditing system, as well as how to conduct audits, and document the results and any nonconformities. It will discuss the value of a good auditing program.
CD/Recorded
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Recorded/CD
Virtual Seminar: Regulatory Modernization in Canada and the US: An Overview of the Key Elements

Virtual Seminar: Regulatory Modernization in Canada and the US: An Overview of the Key Elements

  • Speaker: Felix Amiri
  • Product ID: 705182
  • Duration: 2.5 hrs
This 2.5 hours training will review the key elements of the new food regulations in Canada, the United States and the international marketplace. Get accustomed to new regulatory expectations and be prepared to develop relevant and productive compliance plans.
CD/Recorded
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