As a proven testing and certification service provider, TÜV Rheinland is at your side for all aspects of medical devices and in vitro diagnostics (IVD).

We can support you in the following areas, among others:

- Quality Control / Quality Assurance

- Medical technology

- Contract analysis

- Medical diagnostics

- Medicinal chemistry

- Data Storage

Manufacturers of IVDs face particularly stringent requirements since the adoption of IVDR 2017/746 by the EU. 

TÜV Rheinland is your competent partner for the transition to the updated regulation - as a Notified Body according to IVDR 2017/746 with 40 years of experience in the testing of IVDs.

Our global expertise and presence also make us the right partner for accessing new markets outside of Europe.