Alcis, your partner from idea to market

You have an idea, a concept, a prototype?  Alcis puts its know-how and its facilities at your service to manage your project and get your medical device certified and ready for commercialization.

Alcis benefits from 25-year experience in the medical device field and can help you to get certification for your devices from class I to class III. Alcis can assist you through the launch of your business, the development of your product or the implementation of your quality management system.   We can manufacture your medical devices in a controlled environment (ISO 5 and ISO 7 cleanroom); we can manufacture as an OEM or simply provide you with CE-marked medical devices ready for commercialization.  Our global vision enables us to guarantee a high-quality management for your development and certification projects. Alcis’s strength is to be a small close-knit company with high complementarity between its departments (regulatory, design and manufacturing).


ISO 13485:2016 Medical devices — Quality management systems — Requirements for regulatory purposes.