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Medical Devices Manufacturers


TÜV Rheinland

As a medical devices manufacturer you must ensure that your products meet a variety of requirements and legal regulations. It applies to development, quality management and documentation as well as approval for national and international markets. Our training offers you the expertise required for smooth production processes when it comes to your medical technology and medical devices.

Our qualified trainers will provide you with the necessary knowledge. You will gain an understanding of the complexity of current regulations as part of our seminars and further training courses. Some seminars even allow you to document your acquired qualification with a certificate.

Our portfolio

ErP Directive Evaluation (EU)
ErP Directive Evaluation (EU) 

Understand the impact of your products, processes, and disposal management on the environment.

Contact

Get in contact with us!

Get in contact with us!