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
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
$0
View Details
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
$0
View Details
Recorded/CD
GMP Training Practices to ensure Regulatory Compliance

GMP Training Practices to ensure Regulatory Compliance

  • Speaker: Henry Urbach
  • Product ID: 705077
  • Duration: 90 Min
By attending this webinar, you will gain a better understanding of the regulatory expectations for an effective and GMP-compliant training system. In this webinar your instructor will share with you what he has learned over the past decade of developing and delivering effective GMP training programs as well as from his 25 plus years of working in the Life Science industries.
CD/Recorded
$0
View Details
Recorded/CD
MDR Program conforming to New FDA Guidance

MDR Program conforming to New FDA Guidance

  • Speaker: Edwin Waldbusser
  • Product ID: 705149
  • Duration: 60 Min
FDA, in November 2016, issued a Guidance explaining and clarifying the existing MDR regulation. Many of the details of the MDR regulation were unclear and ambiguous and resulted in nonconformances. This new Guidance attempts to eliminate confusion.
CD/Recorded
$249
View Details
Recorded/CD
Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach

Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach

  • Speaker: Joy McElroy
  • Product ID: 704306
  • Duration: 90 Min
This 90-minute training program is designed for people tasked with performing external audits for their organizations. It is also for those tasked with developing, maintaining and/or improving programs for manufacturing facilities. This includes individuals that have quality management system responsibilities for making general improvements in their organization’s performance specifically related to equipment, processes and documentation.
CD/Recorded
$169
View Details
Recorded/CD
Contamination Control in Pharmaceutical, Biotech and Medical Device Cleanroom

Contamination Control in Pharmaceutical, Biotech and Medical Device Cleanroom

  • Speaker: Jim Polarine
  • Product ID: 705078
  • Duration: 90 Min
This 90-minute webinar will cover general considerations for microbial control for non-sterile manufacturing areas, including attributes of an effective cleaning and disinfection program. Points to consider specifically aimed at oral solid dose (OSD) manufacturers will also be presented, including cleaning and disinfection of both product contact and non-product contact surfaces.
CD/Recorded
$0
View Details
Recorded/CD
Pasteurization Instruments and Records in a Food Processing Facility

Pasteurization Instruments and Records in a Food Processing Facility

  • Speaker: Thomas Perkins
  • Product ID: 704914
  • Duration: 60 Min
The webinar will address the various records required by government agencies in the commercial conversion and packaging of food production. This webinar is designed to allow field level management to competently represent the local process and records as they are intended to satisfy the regulation.
CD/Recorded
$199
View Details
Recorded/CD
Linear Regression Analysis for Medical Device Manufacturing

Linear Regression Analysis for Medical Device Manufacturing

  • Speaker: Daniel O Leary
  • Product ID: 705108
  • Duration: 90 Min
Analyzing processes to understand their operation and implementing improvement is a necessary element in any quality system, but is especially important in medical devices. One of the more important tools is linear regression. Using Excel, you can get the information you need for process improvement.
CD/Recorded
$0
View Details
Recorded/CD
Use of SPC in the Biopharmaceutical industry: use and implementation

Use of SPC in the Biopharmaceutical industry: use and implementation

  • Speaker: Jeffrey Staecker
  • Product ID: 705074
  • Duration: 60 Min
The webinar will describe application of SPC in manufacturing and QC and how to integrate SPC into the Quality System.
CD/Recorded
$0
View Details
Recorded/CD
Quality Control for Microbiological Media and Reagents

Quality Control for Microbiological Media and Reagents

  • Speaker: Todd Graham
  • Product ID: 705060
  • Duration: 60 Min
This webinar will give you the tools you need to maintain a quality supply of media and reagents in a variety of microbiology laboratories. A thorough understanding of the variety of challenges necessary in maintain quality media and reagents will be brought to the fore. This will allow you to perform microbiology testing with confidence.
CD/Recorded
$169
View Details
Recorded/CD
Performing an Effective Out-of-Specification Result Investigation

Performing an Effective Out-of-Specification Result Investigation

  • Speaker: Charity Ogunsanya
  • Product ID: 705064
  • Duration: 90 Min
This webinar will provide the basic understanding of how to conduct a compliant and effective out-of-specification (OOS) result investigation which is critical in preventing product recalls, voluntary and involuntary plant shut down, and FDA 483 findings or warning letter. It will also provide a basic mainframe for the Quality Assurance unit in the final disposition of the affected finished product as well as provide guidance for the different types of OOS investigational systems.
CD/Recorded
$0
View Details
Recorded/CD
Subcontractor auditing (cGMP/Pharma/Med device industries)

Subcontractor auditing (cGMP/Pharma/Med device industries)

  • Speaker: Jan Warner
  • Product ID: 705063
  • Duration: 90 Min
This course will describe the basic principles and requirements for building a supplier audit program. This webinar will provide a framework on which to build your subcontractor auditing program.
CD/Recorded
$0
View Details
Recorded/CD
Packaging and Labeling for Commercial and Clinical Products

Packaging and Labeling for Commercial and Clinical Products

  • Speaker: Peggy Berry
  • Product ID: 704378
  • Duration: 90 Min
This training program will discuss optimizing your packaging design for commercial and clinical products and translating a protocol into effective packaging design. Attendees will learn how to implement an effective artwork change management system. Real-life case studies and dos/don’ts for packaging and labeling for commercial and clinical products will also be discussed.
CD/Recorded
$279
View Details
Recorded/CD
Strategies to Conduct a Successful Method Transfer according to FDA Expectations

Strategies to Conduct a Successful Method Transfer according to FDA Expectations

  • Speaker: Kim Huynh-Ba
  • Product ID: 705059
  • Duration: 90 Min
This webinar discusses how to execute meaningful Method Transfers by selecting appropriate analytical performance characteristics and acceptance criteria, documentation of the transfer process and how to avoid failures.
CD/Recorded
$0
View Details
Recorded/CD
Implementing a Modern Pharmaceutical Quality System

Implementing a Modern Pharmaceutical Quality System

  • Speaker: Steven Laurenz
  • Product ID: 705055
  • Duration: 60 Min
This presentation explores the basic concepts making up an ICH Q10 Quality System approach and steps to properly implement the concepts.
CD/Recorded
$0
View Details
Recorded/CD
Risk of Presence of Objectionable Microorganisms in Biopharmaceutical Production

Risk of Presence of Objectionable Microorganisms in Biopharmaceutical Production

  • Speaker: Henry Urbach
  • Product ID: 705072
  • Duration: 90 Min
This webinar you will discuss how to help your organization get a better handle on what is an “objectionable microorganism, ” exactly how “objectionable” it really is and what you can do to minimize the risk if you find one in your process or product.
CD/Recorded
$249
View Details
Recorded/CD
Risk-based Approach to Biopharmaceutical Method Transfers

Risk-based Approach to Biopharmaceutical Method Transfers

  • Speaker: Jeffrey Staecker
  • Product ID: 705049
  • Duration: 60 Min
This Webinar will discuss how non-compendial biopharmaceutical analytical method transfers can leverage a risk-based approach to address Quality and Regulator concerns. Method transfers using a statistical equivalence approach with tight criteria as frequently suggested by regulators makes it difficult to transfer methods and can result in a high transfer failure rate.
CD/Recorded
$0
View Details
Recorded/CD
Compliance with Brexit's Impact on the Global Pharmaceutical industry

Compliance with Brexit's Impact on the Global Pharmaceutical industry

  • Speaker: Laura Brown
  • Product ID: 705047
  • Duration: 60 Min
Pharmaceutical companies will need to develop strategies for their drug programmes to deal with Brexit. This webinar will provide an essential understanding to help develop a strategy for managing Brexit.
CD/Recorded
$0
View Details
Recorded/CD
Quality by Design

Quality by Design

  • Speaker: Heath Rushing
  • Product ID: 705051
  • Duration: 60 Min
This training program will guide attendees in implementing QbD principles from discovery through product discontinuation. It will also illustrate applying statistics to set specifications and validate measurement systems (assays) and discuss utilizing risk management tools to identify and prioritize potential critical process parameters.
CD/Recorded
$0
View Details
Recorded/CD
Reimbursement Requirements for Designing Innovative Devices

Reimbursement Requirements for Designing Innovative Devices

  • Speaker: Tom Kramer
  • Product ID: 704625
  • Duration: 60 Min
This training program will highlight key metrics needed to convince reimbursement panels of design compliance and discuss how best to implement practices in your development process that ensure acceptance by reimbursement groups.
CD/Recorded
$0
View Details
Best Sellers
You Recently Viewed
    Loading
Copyright © 2026 ComplianceOnline.com
MetricStream
Our Policies: Terms of use | Privacy