The Game - Quality Systems refresher training

An educational and engaging group exercise

The Game makes GMP and Quality Systems refresher training interesting and exciting and activates the participants.

Course description

“The Game” has become much appreciated and allows the participants to actively participate and seek information within the current regulations.
We are convinced that an active and committed course participant learns more, and also contributes with improvement ideas.

The training is an educational and engaging group exercise carried out as a competition where the participants are faced with a number of situations that must treated correctly in relation to current regulations. The participants are working in groups and are acting in different roles (eg. personnel, manager, QA or inspector). At the same time, they also have face different compliance challenges to collect additional points.

It is possible to customize the course content to include your own procedures. Ask for a quotation.

Who should attend

The Game is intended for all personnel who have previously participated in basic- intermediate – or refresher GMP / Quality Systems training and with at least two years of work experience in regulated operations.

There are 4 basic versions:

  • Pharmaceutical production
  • Laboratories
  • API
  • Medical Devices

which can be level-adjusted to the group composition and experience.

The training can be carried out in both mixed and homogeneous groups within e.g. production, QA / QC or other functions with regulatory requirements.


½ day (3 hours)


The Game is best suited for intra-corporate groups with at least 15 and max 25 participants.


Date & Time
Half day
LevelBasic, Intermediate

make an inquiry

In-House Training

This course is available as an In-House Training course. Let us know if you wish to customize a course or if you are a large group with the same requirements.

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Your Instructor(s)

Leading specialist with long experience of training are guiding you through regulations, guidelines, interpretations, requirements and applications.



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