Recently, ESPS has received the certification for the ISO 13485 standard. This is a big step in the broadening of ESPS production activities, now qualified mass production of medical devices is possible for our (future) customers.

ISO 13485 is an ISO standard, published in 2003, that represents the requirements for a comprehensive management system for the design and manufacture of medical devices.

From 2011 mass production of medical devices will take place at the ESPS clean room facility in Almelo.

Click on the picture below to view the certificate.