ComplianceOnline
Join for Free
Signin
Welcome back! Please log in below to continue.
Forgot Password?
New customer? Free Signup
Your Shopping Cart
Contains 0 items
Total: $0.00
View Shopping Cart
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.
Loading....
Recorded/CD
Six Sigma Methodology for Process Validation

Six Sigma Methodology for Process Validation

  • Speaker: Lawrence Mucha
  • Product ID: 700340
  • Duration: 90 Min
This webinar will provide valuable assistance to all regulated companies that need to validate their systems The series will deal with Operational Qualification (OQ), Performance Qualification (PQ), and maintaining a state of validation using statistical methods associated with Six Sigma
CD/Recorded
$149
View Details
Recorded/CD
Overview of Quality by Design

Overview of Quality by Design

  • Speaker: John Avellanet
  • Product ID: 700862
  • Duration: 60 Min
This seminar presents the basics of Quality by Design in such a way as to allow attendees to understand Quality by Design as it applies to their company and their products. Six years after the announcement of the FDA’s cGMP Initiative for the 21st Century, the FDA has finally coalesced on an approach it calls “Quality by Design.” Despite numerous presentations by FDA officials, several pilot programs and the adoption of Quality by Design by the International Conference on Harmonization (ICH), confusion about Quality by Design reigns throughout the pharmaceutical, biotechnology and medical device industries.
CD/Recorded
$149
View Details
Recorded/CD
Quality System Training Requirements

Quality System Training Requirements

  • Speaker: Ronald Schoengold
  • Product ID: 700781
  • Duration: 60 Min
The workshop will provide guidance on the roles and responsibilities of each functional area in the company and how they relate to each other. Each company must demonstrate full implementation of the quality system by providing appropriate training and re-training when necessary, for its employees.
CD/Recorded
$249
View Details
Recorded/CD
Introduction to Statistical Process Control (SPC)

Introduction to Statistical Process Control (SPC)

  • Speaker: Lawrence Mucha
  • Product ID: 700343
  • Duration: 60 Min
This session will introduce advanced control charting for multiple stream processes. We will also introduce control chart analysis and how to select the correct control chart and interpretation and reaction to control chart signals.
CD/Recorded
$249
View Details
Recorded/CD
Applying Lean Documents to a Project - how to create a project file, follow design controls, yet maintain a lean set of project documents

Applying Lean Documents to a Project - how to create a project file, follow design controls, yet maintain a lean set of project documents

  • Speaker: Jose Mora
  • Product ID: 700358
  • Duration: 60 Min
Using the lean document approach, documents are written by the authors with the highest level of expertise, and information is presented in a simple, organized way This webinar explains the use of lean document principles and presents a step-by-step approach to creating a Design History File, a Device Master Record, and other key supporting documents
CD/Recorded
$149
View Details
Recorded/CD
The FDA's Outlook for Quality in Device Manufacturing

The FDA's Outlook for Quality in Device Manufacturing

  • Speaker: James Harris(PhD)
  • Product ID: 700645
  • Duration: 60 Min
This Device Manufacturing webinar provide a understanding of the GMP and Quality requirements for the design, manufacture, storage, distribution, and installation of Medical Devices including the requirements for complaint handling, and servicing.
CD/Recorded
$249
View Details
Recorded/CD
Introduction to statistical Design and Analysis of Experiments (DOE)

Introduction to statistical Design and Analysis of Experiments (DOE)

  • Speaker: Lawrence Mucha
  • Product ID: 700344
  • Duration: 60 Min
This statistical Design and Analysis of Experiments webinar will introduce DOE and process modeling.
CD/Recorded
$249
View Details
Recorded/CD
Designing in Quality via Statistical Process Control

Designing in Quality via Statistical Process Control

  • Speaker: Vinny Sastri
  • Product ID: 700411
  • Duration: 60 Min
This statistical process control training will provide an overview of statistical process control (SPC) describe various types of control charts and how they can be used for trend analysis, defect reduction, product capability assessment. Quality, safety and efficacy must be designed into a product. Quality cannot be inspected or tested in the finished product.
CD/Recorded
$249
View Details
Recorded/CD
Training Requirements and Practices to Assure QSR and ISO Compliance

Training Requirements and Practices to Assure QSR and ISO Compliance

  • Speaker: Jeff Kasoff
  • Product ID: 700316
  • Duration: 60 Min
This Medical device training will instruct on the regulatory requirements of personnel training, and establishment of a training program, including new employee training, methods of training, how to document training. To satisfy QSR and ISO 13485 requirements as well as produce quality products, companies must assure personnel are trained on their routine job practices as well as familiar with requirements that impact them.
CD/Recorded
$249
View Details
Recorded/CD
Management Controls needed for an effective QMS to meet FDA QSR and ISO 13485 regulations

Management Controls needed for an effective QMS to meet FDA QSR and ISO 13485 regulations

  • Speaker: Susan C Reilly
  • Product ID: 700134
  • Duration: 60 Min
This Management control training will provide the principles and practices needed to effectively develop and implement the Management Controls to ensure an effective Quality Management System and to comply with the FDA QS Regulation.
CD/Recorded
$299
View Details
Recorded/CD
Quantitative Approach to User Requirements Risk Assessment

Quantitative Approach to User Requirements Risk Assessment

  • Speaker: Vimarie Ortiz
  • Product ID: 700390
  • Duration: 60 Min
This Risk management training offers a quantitative risk management approach you can use to measure system implementation and enhancement efforts against the criticality and business/regulatory significance of the system.
CD/Recorded
$249
View Details
Recorded/CD
Cleanroom Design, Certification & Classification

Cleanroom Design, Certification & Classification

  • Speaker: Nazia Dar
  • Product ID: 700404
  • Duration: 60 Min
This Pharmaceutical training will also provide attendees with the details and expectation stipulated in ISO 14644 series standards and FDA’s 2004 guidance document for aseptic processing. This seminar is designed to provide a thorough understanding of the principles applied to the design, qualification and operation of cleanrooms.
CD/Recorded
$249
View Details
Recorded/CD
From CAPA to Capability: Shifting the Focus to Profitability

From CAPA to Capability: Shifting the Focus to Profitability

  • Speaker: Barbara Johnson
  • Product ID: 700377
  • Duration: 60 Min
This Quality training will help you look holistically at your quality systems and embrace a continuous improvement approach that will drive quantifiable business benefits. A quick review of your log of corrective and preventive actions can be quite revealing. Many executives have found that their past improvement initiatives only addressed problem areas regarding individual products.
CD/Recorded
$249
View Details
Recorded/CD
CAPA Essentials - core principles and practices needed to implement an effective and efficient CAPA process

CAPA Essentials - core principles and practices needed to implement an effective and efficient CAPA process

  • Speaker: Susan C Reilly
  • Product ID: 700299
  • Duration: 60 Min
This program is designed for the medical device, IVD, and combination product industries This webinar will provide the core principles and practices needed to implement an effective and efficient CAPA process
CD/Recorded
$149
View Details
Recorded/CD
Introduction to Validation of Measurements (Gauge R&R)

Introduction to Validation of Measurements (Gauge R&R)

  • Speaker: Lawrence Mucha
  • Product ID: 700341
  • Duration: 60 Min
This Validation training will provide valuable assistance to all regulated companies that need to validate their systems and will introduce measurement validation using Gauge R&R. Will introduce measurement validation using Gauge R&R. R&R standing for Repeatability and Reproducibility
CD/Recorded
$249
View Details
Recorded/CD
Best Practices for Using Quality Objectives to Drive Meaning

Best Practices for Using Quality Objectives to Drive Meaning

  • Speaker: Michael A Mathe
  • Product ID: 700246
  • Duration: 60 Min
The purpose of this webinar will be to present and identify ways that your quality objectives can Provide and identify improvement opportunities for your system's maintenance and ongoing health. The purpose of this webinar will be to present and identify ways that your quality objectives can Set the tone for using your quality policy statement,Provide a guideline for Top Management’s direction for the organization,Identify improvement opportunities within your system leading to greater reliability.
CD/Recorded
$249
View Details
Recorded/CD
Implementing Quality Management Systems in Small Companies

Implementing Quality Management Systems in Small Companies

  • Speaker: William G Mclain
  • Product ID: 700210
  • Duration: 60 Min
Many small or virtual companies make one of two common mistakes: their Quality Management System (QMS) is either too cumbersome for their operation or they don’t have a quality management system at all Quality management issues facing small, startup or "virtual" companies and identifying all required quality management system elements.
CD/Recorded
$249
View Details
Recorded/CD
Setting up a QSR Compliant CAPA System

Setting up a QSR Compliant CAPA System

  • Speaker: Sue Jacobs
  • Product ID: 700130
  • Duration: 60 Min
In this CAPA training learn how to utilizing multiple data sources to detect actual and potential nonconformities.
CD/Recorded
$249
View Details
Recorded/CD
Effective DOE Strategies to Streamline your Processes for FDA Regulated Environment

Effective DOE Strategies to Streamline your Processes for FDA Regulated Environment

  • Speaker: Jose Mora
  • Product ID: 700165
  • Duration: 60 Min
This DOE (Design of experiments) training focuses on DOE strategies. It is not focused on statistical methods, analysis of variance, and other techniques, but rather the overall approach for successful DOEs.
CD/Recorded
$249
View Details
Recorded/CD
Best Practices on Six Sigma and CAPA Convergence

Best Practices on Six Sigma and CAPA Convergence

  • Speaker: Jose Mora
  • Product ID: 700168
  • Duration: 60 Min
This Quality compliance training will helps in methodologies of Six Sigma and CAPA converging and how to recognize which methodology is best to use for a problem.
CD/Recorded
$249
View Details
Best Sellers
You Recently Viewed
    Loading
Copyright © 2023 ComplianceOnline.com
MetricStream
Our Policies: Terms of use | Privacy