We have conducted over 1,500 web seminars since 2004. We bring you top industry experts who focus their presentations on the How-to aspects of their topic. We've had thousands of people participate representing hundreds of companies around the globe.

Over 3,500 people have participated in one or more of our seminars since 2004

Upcoming LIVE seminars

Scroll down for ON DEMAND SEMINARS AVAILABLE NOW

 

NEW! - Making GMP a Lifestyle in Your Organization, and NOT just a Regulation

Conducted by David Markovitz, Founder and President of GMP Training Systems, Inc.

January 29, 2020  Learn More

 

NEW! - Discover these Simple Hacks to Make Your GMP Training a Success

Conducted by David Markovitz, Founder and President of GMP Training Systems, Inc.

February 19, 2020   Learn More

 

NEW! - Introduction to GMP: An Orientation for New Employees

Conducted by David Markovitz, Founder and President of GMP Training Systems, Inc.

March 25, 2020   Learn More

 

ON DEMAND SEMINARS - AVAILABLE NOW

These one-hour seminars have been recorded in MP4 format. Open and run these files using Windows Media Player or equivalent player. Each MP4 file contains the slides and audio. View in your office or gather your team in a conference room for these high-content seminars conducted by industry experts.

 

Developing and Deploying a Successful GMP Training System: Secrets of a Master Trainer Revealed

Conducted by David Markovitz, Founder and President of GMP Training Systems, Inc.

AVAILABLE NOW   Learn More

 

How to Investigate Deviations and Failures Effectively

Conducted by Gamal Amer, PhD
AVAILABLE NOW   Learn More

 

Implementing FDA's UPDATED Guidance on Quality Metrics

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Developing and Maintaining a Robust Change Control System

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Making GMP a Lifestyle in Your Organization, and NOT Just a Regulation

Conducted by David Markovitz, Founder and President of GMP Training Systems, Inc.

AVAILABLE NOW   Learn More

 

How to Conduct a Successful Supplier Audit: Protecting Your Supply Chain

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Implementing Risk Management (ICH Q9) in the Validation Process

Conducted by Gamal Amer, PhD

AVAILABLE NOW  Learn More

 

Defining Risk and Risk Levels: Implementing ICH Q9: Quality Risk Management

Conducted by Gamal Amer, PhD

AVAILABLE NOW  Learn More

 

How to Implement FDA's Latest Guidance on Process Validation

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

How to Implement FDA's Finalized Guidance on Quality Agreements

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

The How-to Guide to Effective Cleaning and Cleaning Validation

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Environmental Monitoring: Doing it Right!

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

FDA Inspections: What to Expect and How to Prepare

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Implementing CAPA: A Risk Mitigating System

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Validation of HVAC (Heating, Ventilation, and Air Conditioning) Systems: Doing it Right!

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Validation of Water Systems in the Pharmaceutical Industry

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Outsourcing in the Healthcare Industry: Avoiding the Perils and Pitfalls

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Validation and Verification of the Pharmaceutical Supply Chain

Conducted by Gamal Amer, PhD

AVAILABLE NOW  Learn More

 

Stage 3 in Process Validation: How to Maintain the Validated State

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Effective Microbial Control in Pharmaceutical Manufacturing Operations: Preventing Contamination of Drug Products

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Resolving Advanced Cleaning Issues: Multiple Product and Equipment Cleaning, Carryover, and Nonconventional Sources of Contamination

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Effective Equipment Design for Cleaning and Cleaning Validation

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Critical Documents for Successful Cleaning Validation

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Conducting a Gap Analysis of Your Process Validation Program

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Demystifying Design of Experiments (DOE): A Simple and Understandable Pathway to Using DOE

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Master Planning for Validation: Complying with FDA's Latest Guidance on Process Validation

Conducted by Gamal Amer, PhD

AVAILABLE NOW   Learn More

 

Avoid Trouble with FDA: Implementing cGMP for Dietary Supplements

Conducted by David Markovitz, Founder and President of GMP Training Systems, Inc.

AVAILABLE NOW   Learn More

 

Supplier Management Series of four web seminars

NEW - Save $$$ on this package of four outstanding programs - discount for ordering this series

Conducted by Gamal Amer, PhD

AVAILABLE NOW  Learn More

 

NEW! - Introduction to GMP: An Orientation for New Employees

Conducted by David Markovitz, Founder and President of GMP Training Systems, Inc.

AVAILABLE NOW   Learn More

 

NEW! - GMP and Validation Forum: Top industry experts reveal insights into what really matters in GMP and Validation

Conducted by Gamal Amer, PhD and David Markovitz

TBD  Learn More

 

Archived Web Seminars - Click here


 

Archived Web Seminars

All of our Web Seminars are recorded and available on CD or MP3 file along with the handout materials. Click on Review to read the full description of the program.

GMP seminars

Making GMP a Lifestyle in Your Company,
and Not Just a Regulation

David Markovitz


Lessons from Recent FDA Actions

David Markovitz

Developing and Deploying a Successful GMP Training System
Secrets of a Master Trainer Revealed
David Markovitz

Implementing FDA’s Guidance: Quality Systems Approach to Pharmaceutical CGMP Regulations
New Recommendations to Facilitate Modernization of Drug Manufacturing
David Markovitz


Implementing cGMPs for Dietary Supplements
David Markovitz


Calibration in the Laboratory: Getting it Right!!
Jerry Lanese, PhD


Understanding and Implementing FDA's NEW Draft Guidance on Quality Agreements
Gamal Amer, PhD


How to Implement FDA's Latest Guidance on Process Validation
Adopted by FDA January 2011
Gamal Amer, PhD


Environmental Monitoring: Getting it Right!
Gamal Amer, PhD


Demystifying Design of Experiments
A Simple and Understandable Pathway to Using DOE
Gamal Amer, PhD


Implementing Risk Management in the Validation Process - ICH Q9
Gamal Amer, PhD


Risk and the Risk Mitigation Continuum: The GMP Perspective
Gamal Amer, PhD


The How-to Guide to Effective Cleaning and Cleaning Validation
Gamal Amer, PhD


Advanced Cleaning Issues: Multiple Product and Equipment Cleaning, Carryover, and Nonconventional Sources of Contamination
Gamal Amer, PhD


Effectively Implementing CAPA (Corrective and Preventive Action): A Risk Mitigating Quality System
Gamal Amer, PhD


Master Planning for Validation: Complying with FDA's Latest Guidance
Gamal Amer, PhD


Validation Protocol Development and Acceptance Criteria
Gamal Amer, PhD


Validation Protocol Execution and Addressing Deviations
Gamal Amer, PhD


Validation and Change Control: The Validation Life Cycle
Gamal Amer, PhD


ASTM E2500 Consensus Standard: An Overview of a New Approach to Validation
Gamal Amer, PhD


Unraveling the Mysteries of Process Validation: ASTM E2500 Consensus Standard and FDA's New Guidance on Process Validation
Gamal Amer, PhD


Implementing a Risk-based Approach to GMP Compliance
Gamal Amer, PhD


Proven Steps in Reducing Waste in Process Validation
Gamal Amer, PhD


FDA Inspections: What to Expect & How to Prepare
Learning from Other People's Experiences

Gamal Amer, PhD


Outsourcing in the Healthcare Industry
How to Avoid the Perils and Pitfalls

Gamal Amer, Ph.D.


Defining Risk and Risk Levels
Implementing ICH Q9 - Quality Risk Management

Gamal Amer, Ph.D.


Fundamentals of Quality by Design (QbD)
Implementing ICH Q8 - Quality by Design

Gamal Amer, Ph.D.


Engineering Quality by Design (QbD)

Gamal Amer, Ph.D.


GMP, Validation, and Change Control:
Optimizing Key Elements of an Effective Compliance Program

Gamal Amer, Ph.D.


How to Conduct a Successful Supplier Audit: Protecting Your Supply Chain

Gamal Amer, Ph.D.


How to Investigate Deviations and Failures Effectively

Gamal Amer, Ph.D.


Validation of (HVAC) Heating, Ventilation, and Air Conditioning Systems - Doing it Right!

Gamal Amer, Ph.D.


Validation of Water Systems in the Pharmaceutical Industry

Gamal Amer, Ph.D.


Effective Microbial Control in Pharmaceutical Manufacturing Operations: Preventing Contamination of Drug Products

Gamal Amer, Ph.D.


How to Manage Regulatory Inspections: Getting Ready: Pre-Inspection Auditing, Pre-Approval Inspection Preparation, and System-based Inspections
David Inglis, Ph.D.


How to Manage the Inspection Room and the Control (War) Room during Regulatory Inspections
David Inglis, Ph.D.


Staff Training and Preparation for a Regulatory Inspection
David Inglis, Ph.D.


Developing an Effective Response to Regulatory Inspections (FDA and EU)
David Inglis, Ph.D.


How to Effectively Manage Out of Specification (OOS) Results for Pharmaceutical Manufacturers
Laboratory Investigations

David Inglis, Ph.D.


How to Effectively Manage Out of Specification (OOS) Results for Pharmaceutical Manufacturers
Full Scale Expanded Investigations

David Inglis, Ph.D.


Practical and Effective Application of Design Review:
An FDA Requirement for New or Modified Facilities or Systems

Miguel Montalvo