UNI EN ISO 13485:2016 Design, manufacture and testing of sterile and non-sterile medical devices for own brand and third parties.

UNI EN ISO 9001:2015 Design, manufacture and control of sterile and non-sterile medical devices for own brand and third parties; Design, manufacture and control of food supplements for own brand and third parties Design, manufacture and control of cosmetic products for third parties.

Certifying Agency: Bureau Veritas Italia Spa.

Each of our processes is rigorously planned and controlled, from the entry of materials (both raw materials and primary and secondary packaging materials) to the release of the finished product.
The procedures in place ensure a proper management of all processes; they prevent any risks related to product safety and, last but not least, are aimed at complete customer satisfaction. A constant monitoring is also the basis for continuous improvement of the products and services offered.