Fit for the future with the Metecon Academy

As a Metecon team, we have acquired an enormous amount of know-how in regulatory compliance over the past 20 years and anchored this in processes and structures within the company at a very early stage. This means that all colleagues can access and benefit from it quickly and easily.

However, knowledge also grows from experience, and it was also important for us at Metecon to bundle this experience and pass it on - especially to our new colleagues, some of whom are young. After all, it is often experience that gets us to our goal faster and without detours.

We have been cultivating our knowledge management for a long time. In order to add the essential large portion of the experience, the possibility of 1:1 exchange and planned to learn from each other, we came up with an idea in 2017 whose realization was only logical: the Metecon Academy, both for us and for you as a manufacturer of medical devices and IVD.

Take a look around, get to know us!

Since 1999, we have been a strategic partner for our customers and experts in documentation, market access and post-market surveillance of medical devices and IVDs.
Since 1999, we have been a strategic partner for our customers and experts in documentation, market access and post-market surveillance of medical devices and IVDs.


Our trainee program "Regulatory Affairs Manager Medical Devices".

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Individually tailored to your exact topic: In-house workshops Regulatory Compliance.

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Gain new perspectives through intensive exchange with us.

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How you can benefit from the Metecon Academy

Medical technology, like all industries, suffers from a shortage of skilled workers. As a service provider for the again highly specialized regulatory area within medical technology, we had to find a way to equip new team members faster and better with all the know-how that is essential for their job. So we defined topic leaders, knowledge brokers whose job it is to provide their colleagues with what we, as a knowledge society, are urged for: excellence and expertise.

Since 2018, we have been excellently succeeding in this: our trainee program, in which we train to become a Regulatory Affairs Manager Medical Devices, brings our new team colleagues much more quickly into the topic and thus into action; our individual workshops, which take place precisely according to the needs of the respective customer, are in high demand; and our consulting sessions shed light on the darkness and reveal new perspectives and approaches.

Curious? Then let's consider together, without obligation, how we can support you and/or your team.

Every day, we experience the difficult challenges faced by medical device manufacturers: The regulatory requirements are enormous and the team often achieves incredible things despite a heavy workload. Qualified reinforcements are urgently sought - usually in vain because the shortage of skilled workers is clearly reflected in our industry. So how about training your own staff with our support, tailored to your needs? Let's think about it together!
I look forward to hearing from you.

Oliver Schaer - Business Development

Oliver Schaer

Business Development
M +49 1522 8806614

Do you have a question about the Metecon Academy?

Oliver Schaer is looking forward to your message!
Write him directly at

Our academy offer

Efficient training

Until recently, we faced the same problem as many of our customers: Regulatory Affairs experts are hard to find, and the time needed to train (lateral) entrants are extremely long...
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Customized workshops

Each of our workshops imparts sustainable knowledge and know-how in the areas of technical documentation, regulatory affairs and QM and is always tailored to your needs...
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Goal-oriented consulting

Your topic is not yet clearly enough defined for a workshop? Nevertheless or you would like to discuss it with other experts? Maybe just to get new perspectives?...
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