YES is an independent and autonomous service provider with outstanding expertise 

• in the area of drug development, with special reference to regulatory affairs in the European Union – before, during and after marketing authorisation
• in the marketing authorisation and lifecycle management of medicinal products in Emerging Markets
• in the field of CE marking and the international approval of medical devices.

We are a team of more than 120 employees working in the areas of biology, chemistry, engineering, food chemistry, medicine, nutritional science, pharmacy, toxicology and veterinary medicine. This enables us to respond to your project requirements flexibly, professionally and at short notice.

Our experienced team in Karlsruhe carries out maintenance activities for medicinal products for human use and takes care for drugs for veterinary use:

Marketing authorisations in Austria are handled by:

The team at Medical Device Services GmbH supports you with regard to medical devices and in vitro diagnostic products. If you have any questions relating to regulatory compliance and quality management, please contact: