Introduction to GAMP 5

How to optimize the quality and time spent developing your computerized systems by using Good Automated Manufacturing Practice (GAMP). This course is designed to provide you with targeted knowledge of GAMP 5 methods and their practical application to ensure product quality, data integrity and patient safety.

Who can participate?

The course is for engineers, technicians, chemists and others who work with or are users of computerized systems in the pharmaceutical industry:
Automation and IT engineers.
Project engineers and managers.
QA employees and managers.
IT managers.
Process engineers and chemists.
Machine builders and robot suppliers.

Course overview

Confirm Knowledge Center
Havnevej 1, 1 tv. 4000 Roskilde
Danish

Prerequisites to participate

There are no prerequisites other than an interest in understanding how GAMP as a tool can benefit suppliers of automated systems that must comply with current GMP regulations.

Read more about the course

Introduction to GAMP 5

Good Automated Manufacturing Practice (GAMP) provides a logical and systematic approach to categorizing, documenting and risk assessing automated systems. In this course, you will gain targeted knowledge on how GAMP 5 methods can help you ensure that product quality, data integrity and patient safety are in order in your computerized systems. The course material is updated with content from the 2nd edition of GAMP5 A Risk-Based Approach to Compliant GxP Computerized Systems published by ISPE in August 2022. Computer System Validation (CSV) is becoming an increasingly important part of the pharmaceutical industry as more production is managed digitally.

Course information

Teaching method

The teaching is a mix of theory and practice, with dialog and discussions based on both student experience and industrial practice. We are always striving to improve our courses and therefore encourage evaluations at the end.

Course highlights

On the course you will achieve:

Understanding GAMP 5 to create clear and measurable URSs, minimizing misunderstandings and errors.
Knowledge of software categorization and risk management.
Overview of necessary documentation and how to use it effectively.
Insights on optimizing skills and collaboration.

Course program

After the course

Reviewed current GAMP 5 rules and guidelines.
Learn how to create relevant documents and plan development and testing phases.
Understanding issues at different lifecycle stages and complexity levels.
The ability to manage risks related to patient safety, product quality and data integrity.

Instructors on the course

Katrine Rivière

In addition to teaching, Katrine works as Engineering Manager at Confirm. Her interest in sharing methods and concrete tools is based on Katrine's own experience as a consultant in the pharmaceutical industry. The course participants particularly value her ability to understand customers' problems, as well as her ability to make complex problems concrete and show examples of how to solve them operationally.

Jeppe Lunde Schmidt

Jeppe works in our validation team on a daily basis. He has GMP experience from several large remodeling projects in pharmaceutical packaging plants and countless validations of everything from simple transmitters to large complex IT systems. He has produced and read a wide variety of documentation and has visited companies and sites across the country. He has worked with manufacturers of both pharmaceuticals and medical devices and incorporates his experience in the industry into his teaching. Jeppe has several years of teaching experience and teaches several of our other courses, including GAMP5 and Data Integrity.

Testimonials from learners


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If you have any questions regarding our courses, our employee Sabrina is ready to help you. Contact Sabrina