SSI Diagnostica takes pride in ensuring the best quality in both our production facilities and finished products, as well as in our customer service and in providing instruction in the use of our products.

SSI Diagnostica's development, production and sale of in vitro diagnostics is quality controlled and certified in accordance with ISO 13485. Products that fulfil the requirements of Council Directive 98/79/EEC of 27 October 1998 on in vitro diagnostic medical devices are CE-certified.

When we develop a new product, we always spend the time required to ensure that we launch efficient and user-friendly products to our customers. This means that our products have always been subject to field tests prior to being launched. When we sell a product, we offer training courses, to ensure the best understanding and use of our products.

Our customers' opinions and experiences with our products mean a lot to us, as this is how we best develop and improve our products and procedures. Therefore, all inquiries, all praise and blame from our customers and users are registered and actively used.