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Online GMP Training Courses

The Cost of Quality and Its Value to the Organization

Date: May 12, 2021

Time: 10:00-11:30 CET (90 minutes)

Learn a systematic process of implementing and assessing the Cost of Quality (COQ) using Six Sigma methodology to plan future projects or showcase your current value to the organization.

Workshop: Deviations and Issue Management Systems

Start date: May 18, 2021

End date: May 19, 2021

Time: 09:00-13:30 (CEST)

In this workshop you will master the essential elements for investigating deviations that arise during the product life cycle of medicinal products and learn how to document and address deviations much more effectively.

Workshop: Root Cause Analysis

Start date: June 1, 2021

End date: June 4, 2021

Time: 09:00-13:30 (16 hours)

This interactive and engaging 16-hour online workshop will help you master the essential elements of a Root Cause Analysis. By the end of this hands-on workshop, you will have the right tools and knowledge to investigate any issue that will arise within a product’s life cycle. The result- fewer repeating deviations, better KPIs, and more time to concentrate on the important projects.

Learn about the GxP Data Integrity and ISO 27001 access management requirements. And get insight into current security concerns and best practice approaches to handling the risks inherent in poor access configuration management in the age of digitalization.

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(Contact us for private sessions)

How To Write An SOP That People Would Love To Follow

Date: May 5, 2021

Time: 10:00-12:00 CET (120 minutes)

Every GMP professional must write or review SOPs at some point in their career. In this webinar, you will learn how to write excellent and SOPs that are user-friendly and GxP compliant.

How to Pick the Right Tools and Execute a Successful Root Cause Analysis

Date: April 29, 2021

Time: 10:00-11:30 CEST (90 minutes)

Gain an enhanced understanding of how to investigate issues efficiently, which deviations to address first, and how. By the end of the webinar, you will be confident that you know how to investigate failures to complete a practical root cause analysis, eliminating 80% of recurring deviations by identifying and implementing adequate corrective actions.

Workshop: Deviations and Issue Management Systems

Start date: April 13, 2021

End date: April 14, 2021

Time: 09:00-13:30 (CEST) - Registration for this date is closed. New session in May.

In this workshop you will master the essential elements for investigating deviations that arise during the product life cycle of medicinal products and learn how to document and address deviations much more effectively.

QA and CSV Effective Problem Solving Strategies During System Delivery

Date: March 24, 2021

Time: 10:00-11:30 CET (90 minutes)

Learn strategies for building effective working relationships between QA and CSV representatives to overcome common validation challenges, which will improve system delivery, compliance, and harmony at the workplace.

How To Continually Improve Your Quality System

Date: January 11, 2021

Time: 10:00-11:30 CET (90 minutes)

In this live GMP training webinar, you will learn how to process corrective and preventive actions (CAPAs) effectively and maintain an efficient continual improvement system.

How To Take Control Over Your Deviations

Date: December 8, 2020

Time: 10:00-11:30 CET (90 minutes)

This webinar will help you change your mindset on the importance of handling correctly issues that arise during your product’s lifecycle. You will learn how to approach and manage deviations effectively. As a result, you will become more efficient, have fewer repeating deviations on your hands, and comply better with regulations.

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What are your requirements?

Feel free to contact us, and we will be more than happy to answer all of your questions and address all your needs. 

Wait, don't leave empty-handed!​

Download our free Ultimate FMEA Guide, which is dedicated to GMP and pharma professionals.

This extensive yet simplified guide to Failure Mode and Effects Analysis (FMEA) will help you master one of the most vital instruments in your risk management toolbox.

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