Home
Start selling your products without delay.
Tecurat supports manufacturers of medical devices.
With many years of experience in development, quality management, regulatory affairs and project management we support your projects.
- E-Learning
- Auditing
- Consulting
- save time

Start implementing immediately and close gaps
With our free checklist package, you will gain more time and
start implementing instead of preparing.
Use the prepared contents from the MDR attachments:
The Medical Device Regulation
Do you want to use your time effectively?
Are you professionally involved with MDR?
Do you want to start implementation instead of reading guidelines?
We are using 3 pillars to break down the contents into understandable parts

Overviews
Using explanations, excerpts and examples, you can quickly analyze the contents of the MDR.

Instructions & CheckLists
You will receive instructions and checklists for the most important sections and requirements in order to prepare yourself efficiently.

Videos & explanations
Where it is possible according to the current status, you will receive examples of implementation and preparation. The course will continue to grow in the future, and will include new and current MDR topics.
Statements from our customers
Aktuelle Fachbeiträge
Halten Sie sich auf dem laufenden mit Tips & Analysen für Experten in der Medizintechnik.

MDR and UDI
The MDR - the Medical Device Regulation - has been implemented. It has been in force since 25 May 2017, with a 3-year transition period. The MDR must therefore be fulfilled by all medical device manufacturers (more precisely: distributors) from 26 May 2020.According to current changes this deadline was extended
Make an appointment now.
We would be happy to contact you.
Leave your email address and we will contact you shortly.