upcoming public virtual Classes

August 12, at 17:00 CEST

A Best Practice Approach For a Compliant Annex 1 Biocide Qualification

Learn about the most important aspects of biocide qualification to minimize workload and comply with the regulator’s expectations.

A Best Practice Approach For a Compliant Annex 1 Biocide Qualification

Length: 90 minutes

Sessions: Private and public

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Live Online Classes

Virtual Class

Good Manufacturing Practices (GMP) Introduction Course

Learn what GMP is and how it came to be. The course will cover the pharmaceutical quality system and the main regulations to allow you and your company to stay compliant.

Good Manufacturing Practices (GMP) Introduction Course

Length: ~8 hours

Sessions: Private and public

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Virtual Class

GMP Refresher and New Trends

This course will help you refresh your knowledge of pharmaceutical quality systems and allow you to familiarize yourself with the latest trends and regulations.

GMP Refresher and New Trends

Length: ~8 hours

Sessions: Private and public

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Virtual Class

GMP Intro Course for Recruitment Consultants

This course will help you understand the industry you recruit for much better. You will learn about the pharmaceutical industry and the most important factors of GMP. .

GMP Intro Course for Recruitment Consultants

Length: ~8 hours

Sessions: Private and public

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Virtual workshop

Deviations and Issue Management Systems

In this interactive workshop, you will learn the best practice framework to deal efficiently with deviations that occur throughout the product's life cycle.

Deviations and Issue Management Systems

Length: ~8-10 hours

Sessions: Private and public

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Can’t find the courses you are looking for? No problem! 
We specialize in creating customized training courses for our customer’s needs. 

UPCOMING WEBINARS

There are no upcoming events.

Past Events:

(Contact us for private sessions)

Workshop: Deviations and Issue Management Systems

Date: July 8, 2021

Time: 09:00-19:00 CEST (9-10 hours)

In this intensive full-day 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.

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.

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.

Workshop: Deviations and Issue Management Systems (Session closed for registration)

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.

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.

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.

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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