We have been working for internationally active implant manufacturers for over 20 years. During this time we have acquired extensive experience in the field of implants production.
Being certified according to ISO 13485/CRF 21 PART 8 in 2009, we were able to supplement our know-how with the qualification, validation and risk analysis processes which are indispensable for the production of this product category. Since then we have had many years of valuable experience in applying these processes in the production of implants. Every year our employees partake in a special training course followed by a test to verify the knowledge they have gained, in order to guarantee a high degree of reliability in the application of the processes at all stages of value creation.