Regulatory excellence for medical devices (MedDO/MDR) and in vitro diagnostics (IvDO/IVDR).

With us, you can rely on a team of 60 Metecon experts with comprehensive skills and, as a company, more than 20 years of experience with medical devices and in vitro diagnostics (IVDs) in the areas of technical documentation, verification, validation, market access and market monitoring (PMS, PMCF/PMPF).

We help you avoid limits and implement your projects successfully. Whether you are looking for short-term support or a long-term partnership: We are there to assist you in a reliable and solution-oriented manner. Our team is diversified; all employees are experts in their field. This makes us flexible and allows us to react quickly to your requests.

Our experts from all relevant fields are engineers and scientists. This diversity of expertise allows us to provide you with the best support quickly for projects of any size and on any topic. The regulatory requirements of the market are our trademark. We make sure that you can proceed safely and successfully.

Improve your market success with our professional support - Contact us!

Your contact persons are looking forward to hearing from you

With safety guaranteed: MDR, IVDR, MedDO, IvDO & Co.

In times like these, when so much is changing in terms of regulations, we offer you the assurance that we always keep an eye on all the necessary requirements for your product.

The transition towards the Medical Devices Ordinance (MedDO or (EU) 2917/745, MDR) and the In Vitro Diagnostics Ordinance (IvDO or (EU) 2017/746, IVDR) poses particular challenges for all of us. At Metecon, we are well-prepared to help you meet these requirements with ease - no matter if for new products or for devices already on the market. Our goal is to ensure that you successfully place your medical devices/in vitro diagnostics (IVDs) for as long as possible in your target markets.

A journey through the Metecon world